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Website content last updated on Tuesday 2019-12-03
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cGMP Validation LLC cGMP Validation is a full service validation firm offering services for the pharmaceutical, bulk pharmaceutical, animal health, biotechnology, biologics, medical device and medical diagnostic industries.
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Compli - a Commissioning, Validation, cGMP and Regulatory Compliance Consulting Company A commissioning, validation, cGMP and regulatory compliance consulting services company with exceptional expertise and experience in project scoping, execution and solutions.
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Compli - a Commissioning, Validation, cGMP and Regulatory Compliance Consulting Company A commissioning, validation, cGMP and regulatory compliance consulting services company with exceptional expertise and experience in project scoping, execution and solutions.
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NAP by CGMP - Leader français des arts de la table éphémère Créateur et fabricant de serviettes, nappes, sets, rouleaux en papier et autres accessoires. NAP, habilleur de tables depuis 65 ans.
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Website is under construction GMP news
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GMP-Creative Biolabs: One-stop full-GMP service provider GMP-Creative Biolabs provides one-stop customer-oriented services including biopharmaceutical contract R&D, process development, cGMP manufacturing, QA & QC solutions for scientific research, preclinical, clinical and commercial supply.
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GMP-Creative Biolabs: One-stop full-GMP service provider GMP-Creative Biolabs provides one-stop customer-oriented services including biopharmaceutical contract R&D, process development, cGMP manufacturing, QA & QC solutions for scientific research, preclinical, clinical and commercial supply.
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GMP, Good Manufacturing Practice, SOP Quality Documents for FDA | EU | EMEA | cGMP High Quality Pharmaceutical Quality Documents: ✅ GMP Checklists, ✅ Standard Operation Procedures, ✅ Master Plans and ✅ Quality Contracts. For Regulatory Guidance, Compliance with FDA | EU | EMEA | cGMP. ✅ Direct download. Written by Pharmaceutical industry specialists.
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Gourmet Food Safety Consultancy for SAC HACCP Doc 2, ISO 22000, BRC, cGMP Gourmet Food Safety Consultancy, singapore, HACCP, food, safety, gourmet, ISO 22000, BRC, cGMP, Lawrence Low, Hazard Analysis, GMP, SAC, SIFST, AVA, standards, audit
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GMP, Good Manufacturing Practice, SOP Quality Documents for FDA | EU | EMEA | cGMP High Quality Pharmaceutical Quality Documents: ✅ GMP Checklists, ✅ Standard Operation Procedures, ✅ Master Plans and ✅ Quality Contracts. For Regulatory Guidance, Compliance with FDA | EU | EMEA | cGMP. ✅ Direct download. Written by Pharmaceutical industry specialists.
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cGMP Consulting, Inc. (current Good Manufacturing Practices) cGMP Consulting is a Chicago based engineering firm providing a range of services to FDA regulated industries. Helping clients stay compliant, since 2001.
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cGMP, cGLP, cGEP, Normas Iso, Farmacéutica, Salud, Cosmética, Alimentos - Cercal Group Somos expertos en servicios de capacitación y consultoría cGMP, cGLP, cGEP, Normas ISO, aplicada industrias como Farmacéutica, Alimentos, Salud y otras
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PharmaSys, Inc. PharmaSys specializes in cGMP, GLP and GCP regulations. We provide timely, cost effective compliance and validation solutions to our customers'' challenges.
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PharmaSys, Inc. PharmaSys specializes in cGMP, GLP and GCP regulations. We provide timely, cost effective compliance and validation solutions to our customers'' challenges.
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Home - Cytovance Biologics Cytovance® Biologics is a contract development manufacturing company specializing in the cGMP production of therapeutic proteins and antibodies from mammalian cell culture, microbial fermentation, transgenic processes, and small scale “flex suite” programs. In addition, Cytovance offers process development services, cell line development, purification development, stability testing, and regulatory support services – all from its Oklahoma City state-of-the-art facilities. Cytovance partners with clients to provide integral pathways in converting novel protein discoveries into lifesaving therapies and diagnostics. Cytovance® Biologics operates out of four separate facilities in Oklahoma City, Oklahoma. Three of the four facilities house our cGMP manufacturing with each building properly segregating our Mammalian, Microbial, and Transgenic / Flex suite clientele. All three of these facilities have been designed to operate as multi-product and are custom-designed for cost-effective multi-product cGMP production of therapeutic proteins. Each designed to meet global regulatory standards. Our 50,000 sq. ft. Mammalian facility features primary production in cell culture suites utilizing single-use bioreactors at 50L, 100L (w/v), 200L, 250L, and 1,000L scale and Stainless Steel bioreactors at 100L, 500L (w/v), 1,000L scales (5000L scale coming online in late 2016). Recovery and purification is undertaken in adjacent independent Purification suites. Our second facility houses six unique cGMP manufacturing suites intended to produce specialized therapeutic products. These “Flex” suites can quickly be reconfigured to run a variety of different biologics platforms. This facility also houses our clinical automated vial filling operations, Process and Analytical Development laboratories, and our administrative offices. Our third and newest facility houses our GMP warehouse and our Microbial manufacturing capabilities. Our Microbial scales include cGMP fermentation processes at the 14L, 100L, 200L, and 1000L (Q1 2016) scales. This facility also includes all applicable cell processing and downstream recovery process suites. Our fourth facility houses our Quality Control Laboratories.
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Homepage - Flamma S.p.A. Flamma is a fully integrated CMO that has two cGMP facilities in Italy & a cGMP/non-cGMP facility in China. Flamma does custom synthesis and manufacturing of APIs, RSMs, and high value chiral building blocks such as amino acids. Flamma can manufacture chiral intemediiates at MT scale.
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Home - Cytovance Biologics Cytovance® Biologics is a contract development manufacturing company specializing in the cGMP production of therapeutic proteins and antibodies from mammalian cell culture, microbial fermentation, transgenic processes, and small scale “flex suite” programs. In addition, Cytovance offers process development services, cell line development, purification development, stability testing, and regulatory support services – all from its Oklahoma City state-of-the-art facilities. Cytovance partners with clients to provide integral pathways in converting novel protein discoveries into lifesaving therapies and diagnostics. Cytovance® Biologics operates out of four separate facilities in Oklahoma City, Oklahoma. Three of the four facilities house our cGMP manufacturing with each building properly segregating our Mammalian, Microbial, and Transgenic / Flex suite clientele. All three of these facilities have been designed to operate as multi-product and are custom-designed for cost-effective multi-product cGMP production of therapeutic proteins. Each designed to meet global regulatory standards. Our 50,000 sq. ft. Mammalian facility features primary production in cell culture suites utilizing single-use bioreactors at 50L, 100L (w/v), 200L, 250L, and 1,000L scale and Stainless Steel bioreactors at 100L, 500L (w/v), 1,000L scales (5000L scale coming online in late 2016). Recovery and purification is undertaken in adjacent independent Purification suites. Our second facility houses six unique cGMP manufacturing suites intended to produce specialized therapeutic products. These “Flex” suites can quickly be reconfigured to run a variety of different biologics platforms. This facility also houses our clinical automated vial filling operations, Process and Analytical Development laboratories, and our administrative offices. Our third and newest facility houses our GMP warehouse and our Microbial manufacturing capabilities. Our Microbial scales include cGMP fermentation processes at the 14L, 100L, 200L, and 1000L (Q1 2016) scales. This facility also includes all applicable cell processing and downstream recovery process suites. Our fourth facility houses our Quality Control Laboratories.
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Homepage - Flamma S.p.A. Flamma is a fully integrated CMO that has two cGMP facilities in Italy & a cGMP/non-cGMP facility in China. Flamma does custom synthesis and manufacturing of APIs, RSMs, and high value chiral building blocks such as amino acids. Flamma can manufacture chiral intemediiates at MT scale.
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TTGP SOLUTION GROUP Thiết kế thi công nhà máy, Thi công HVAC, Thi công phòng sạch, Tư vấn ISO, GMP, CE..., đào tạo ISO, cung cấp thiết bị sản xuất thí nghiệm, chuyển giao công nghệ iso, tư vấn mỹ phẩm, tư vấn đủ điều kiện sản xuất mỹ phẩm, tư vấn cgmp, tư vấn nhà máy mỹ phẩm cgmp
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Home Business, Validation Engineer, GMP, GAMPS, DeltaV, IQ, OQ, PQ, Contract, Pharmaceutical, cGMP, IQ, OQ, PQ, Automation Validation, Process Validiation, Vaccines, Cleaning Validation, Packaging Validation, Automation, Computer, Equipment, Process Control, Process, QIP, CIP, SIP , WIP, Blister, Bottle lines, IMA Qualified, LCAC Gearbox Preservation, AOE-6 ILS, LSA Support, YF-120 Testing, QIP, CIP, TQM, Standardized process procedures, cGMP, GAMP, 21 Part 11 Qualifications, Operation and Maintenance Manual, GIV, Gulfstream, UPS B727 Manual, Columbia Gas O&M Manual, D sheets, E sheets, Illustrated Parts breakdown, Functional Block Diagrams, Verification, AmeriGraf, engine test, electro-mechanical testing, military contract support, commerical contract supportTechnical manual development, OQ development, OQ execution, technical services, engineering procurement support, URS, DDS, DS, FRS, FS, FDS, VMP, VP, Traceability matrix development, Dee Howard, development, execution, PNR, IMRs, Decrepancy Reports
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TTGP SOLUTION GROUP Thiết kế thi công nhà máy, Thi công HVAC, Thi công phòng sạch, Tư vấn ISO, GMP, CE..., đào tạo ISO, cung cấp thiết bị sản xuất thí nghiệm, chuyển giao công nghệ iso, tư vấn mỹ phẩm, tư vấn đủ điều kiện sản xuất mỹ phẩm, tư vấn cgmp, tư vấn nhà máy mỹ phẩm cgmp
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TTGP SOLUTION GROUP Thiết kế thi công nhà máy, Thi công HVAC, Thi công phòng sạch, Tư vấn ISO, GMP, CE..., đào tạo ISO, cung cấp thiết bị sản xuất thí nghiệm, chuyển giao công nghệ iso, tư vấn mỹ phẩm, tư vấn đủ điều kiện sản xuất mỹ phẩm, tư vấn cgmp, tư vấn nhà máy mỹ phẩm cgmp
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Action Labs - Call 1 (714) 630-5941 Sentinel Vitamins from Action Labs has been based in the United States since 1964 Action Labs has been serving customers around the world for 50 years. Quality you can Trust. All products are manufactured under Current Good Manufacturing Practice regulations (cGMP). Great Prices on vitamins and supplements, health products, Men''s Products, Women''s Products, Children''s Products. Shop online or call 1 (714) 630-5941. Action Labs is based in the United States and has been serving customers around the world for 50 years. Quality you can trust. All products are manufactured under Current Good Manufacturing Practice Requlations (cGMP).
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Action Labs - Call 1 (714) 630-5941 Sentinel Vitamins from Action Labs has been based in the United States since 1964 Action Labs has been serving customers around the world for 50 years. Quality you can Trust. All products are manufactured under Current Good Manufacturing Practice regulations (cGMP). Great Prices on vitamins and supplements, health products, Men''s Products, Women''s Products, Children''s Products. Shop online or call 1 (714) 630-5941. Action Labs is based in the United States and has been serving customers around the world for 50 years. Quality you can trust. All products are manufactured under Current Good Manufacturing Practice Requlations (cGMP).
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QSI: Quality Systems Integration, LLC. QSI specializes in providing practical and cost-effective solutions to design, document, and validate your facility, utility systems, computerized systems, software, and equipment in a CGMP compliant state while maintaining and improving FDA and/or European (ISO) regulatory compliance.
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Is that pen CGMP Compliant? - GMPPENS
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Home: KBN Certification System ISO 9001 :2015, ISO 14001 : 2015, ISO 18001 : 2007, ISO 27001 : 2013 - ISMS, ISO 22000 : 2005 - FSMS, ISO 13485 : 2016,ISO 10002 : 2016 MDQMS, TS 16949: 2016, HACCP, HALAL, CGMP, GMP, BRC, GOTS, ISO Reach, ISO CE Mark, ISO ROHS, ISO FCC, Organic Certification, ISO 29001, ISO 31000
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Home Page Validation and cGMP compliance services for Pharmaceutical, Biotechnology and Medical Device Inductries. Web site of U.S. Validation Services Inc.
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World Wide Label | Driven By Technology Founded in 2000, Worldwide Label & Packaging is an ISO 9001:2008 certified and cGMP compliant converter of specialty packaging for leading consumer and healthcare products companies. Capabilities include 8-color Flexographic and UV Flexo printing, precision rotary die cutting, film & label attachments, and leaflet folding.
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Home Page Validation and cGMP compliance services for Pharmaceutical, Biotechnology and Medical Device Inductries. Web site of U.S. Validation Services Inc.
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On-Demand ISO 9001 training ISO 14001, ISO 13485, IATF 16949, AS9100D, GMP CALISO offers on-demand ISO 9001:2015 and ISO 14001:2015 Auditor training. Courses enables certification on ISO 14001, ISO 13485, cGMP, GLP, GMP.
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德固工業股份有限公司 - Ucrete 工業地板,食品廠地板,製藥廠地板專業團隊 德固工業股份有限公司,工業地板,食品廠地板,製藥廠地板,Ucrete:符合CAS,Haccp,CGMP,FGMP,耐溫抗凍,耐沖刷洗,耐藥品抗菌地板,調理油炸區,空廚,中央廚房,充填包裝區,防滑地板,彩砂地板,EPOXY環氧樹脂:無塵無縫地板,食品級EPOXY,抗靜電地板,ABS進口工業級自平泥,快速整平,超平耐磨,FRP耐酸鹼內襯:廢水池,污水池,酸洗池,電鍍槽內襯,重防蝕地床:耐溫耐酸鹼地板
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CE&IC is cGMP Engineering Design for pharmaceutical and biotechnology CE&IC is a full service cGMP engineering and design firm established in 1984 and focused on serving our pharmaceutical and biotechnology clients
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Welcome to Pharmaceutical Outsource Solutions, Inc. Pharmaceutical Outsource Solutions, Inc. is a consulting service specializing in the logistics of setting up and managing GLP and cGMP outsourced testing.
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Cell line development, CHO protein, cGMP MCB/WCB|ExcellGene The science-driven CDMO for protein expression services. High-quality CHO/HEK protein from transient & stable expression, upstream processing & downstream processing, stable cell line generation, recombinant protein production, cGMP master cell banking and VLP production.
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Welcome to Our Website :: We International Quality Systems An ISO Consultancy & Training Providing Co. in INDIA If you are Looking for Quality Certification Consultancy/Quality System Consultancy / Training & Seminars Consultancy for your organization on ISO 9001:2008 ISO14001: 2004 OHSAS18001: 2007 ISO/TS 16949:2009 ISO 27000 ISO 22000 HACCP SA 8000 GHP/cGMP/GMP/ WHO-GMP BIS (ISI) Marking CE MARK UL Certifications School Accreditation Soft Skills Six Sigma Kaizen Lean Manufacturing Total Quality Management (TQM) Poka Yoke Quality Circles Benchmarking Total Preventative Maintenance Statistical Process Control (SPC) INTERNATIONAL QUALITY SYSTEMS Head Office: A-33, Keshav Nagar, Numaish Camp, Saharanpur-247001, Tel: +91-132-2660077, 3295777 NCR Office: D-21, Second Floor , Sector 27 +91-93132 97100 Mumbai Office: A-602, Amaltas Housing Co-Operative Society, Juhu-Versova Link Road, Mumbai , +91-22-32951781 E-mail: info@iqsglobal.com, promo@iqsglobal.com Website: http://www.iqsglobal.com
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PCD Franchise Pharma Company | PCD Pharma Distributors | Hi-Cure Biotech Hi-Cure Biotech PCD based Pharma franchise Company trading gynae, ortho, dental, injectable cgmp products looking for pcd pharma distributors across India to franchise its quality and cost effective formulations.
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CE&IC is cGMP Engineering Design for pharmaceutical and biotechnology CE&IC is a full service cGMP engineering and design firm established in 1984 and focused on serving our pharmaceutical and biotechnology clients
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Is that pen CGMP Compliant? - GMPPENS
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Welcome to The AquaMarine Group, Inc. Since 1996, The AquaMarine Group, Inc.’s services have been sought and retained by pharmaceutical firms, to furnish expertise in the areas of regulatory review, application writing, cGMP compliance/mock pre-approval audit services, R&D portfolio analysis, contracted management services, and new product/technology evaluation and promotion. Services furnished to clients include not only review and commentary, but have also included project management for a number of significant filings.
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Validation Online | Drugs | Device | Bio-tec | Machine | Dental | cGMP Validation Online retails cGMP compliant Validation packages containing VMP, URS, DQ, IQ, OQ & PQ. Or the new VrrP & 4Q two document validation Package.
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A Dietary Supplements Manufacturer | cGMP OEM - Arcman Pharma Arcman Pharma is a contract manufacturer and private label manufacturer for Vitamin, Fish Oil, Protein, Maca, Q10, Phytoplankton, Herbs and other dietary supplements. We offer comprehensive services for nutritional products manufacturing including tablet press, encapsulation, bottling, granulation, blending, powder filling, (multi) packaging and more.
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A Dietary Supplements Manufacturer | cGMP OEM - AMF Pharma AMF Pharma is a contract manufacturer and private label manufacturer for Vitamin, Fish Oil, Protein, Maca, Q10, Phytoplankton, Herbs and other dietary supplements. We offer comprehensive services for nutritional products manufacturing including tablet press, encapsulation, bottling, granulation, blending, powder filling, (multi) packaging and more.
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德固工業股份有限公司 - Ucrete 工業地板,食品廠地板,製藥廠地板專業團隊 德固工業股份有限公司,工業地板,食品廠地板,製藥廠地板,Ucrete:符合CAS,Haccp,CGMP,FGMP,耐溫抗凍,耐沖刷洗,耐藥品抗菌地板,調理油炸區,空廚,中央廚房,充填包裝區,防滑地板,彩砂地板,EPOXY環氧樹脂:無塵無縫地板,食品級EPOXY,抗靜電地板,ABS進口工業級自平泥,快速整平,超平耐磨,FRP耐酸鹼內襯:廢水池,污水池,酸洗池,電鍍槽內襯,重防蝕地床:耐溫耐酸鹼地板
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Tafaseel Engineering Est. (TEE) Amman, Jordan, Stainless Steel Piping Systems, American Welding Society, TEE, Tafaseel, Engineering,Tanks, Pipes, Pumps, Valves, Control, PW-WFI-PSG, Water Systems, cGMP, ,EP,USP, JP ,ISPE, FDA requirements
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Validation Online | Drugs | Device | Bio-tec | Machine | Dental | cGMP Validation Online retails cGMP compliant Validation packages containing VMP, URS, DQ, IQ, OQ & PQ. Or the new VrrP & 4Q two document validation Package.
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Avista Pharma Solutions, CDMO Avista is a CDMO that offers services from early stage discovery, API & Drug Product development & cGMP manufacturing to stand-alone testing support.
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On-Demand ISO 9001 training ISO 14001, ISO 13485, IATF 16949, AS9100D, GMP CALISO offers on-demand ISO 9001:2015 and ISO 14001:2015 Auditor training. Courses enables certification on ISO 14001, ISO 13485, cGMP, GLP, GMP.
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Avista Pharma Solutions, CDMO Avista is a CDMO that offers services from early stage discovery, API & Drug Product development & cGMP manufacturing to stand-alone testing support.
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Home: KBN Certification System ISO 9001 :2015, ISO 14001 : 2015, ISO 18001 : 2007, ISO 27001 : 2013 - ISMS, ISO 22000 : 2005 - FSMS, ISO 13485 : 2016,ISO 10002 : 2016 MDQMS, TS 16949: 2016, HACCP, HALAL, CGMP, GMP, BRC, GOTS, ISO Reach, ISO CE Mark, ISO ROHS, ISO FCC, Organic Certification, ISO 29001, ISO 31000
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Industry-Leading cGMP Cleanroom Supplies & Solutions | SPS CleanTech Don’t let downtime threaten your production. SPS CleanTech provides industry-leading cGMP cleanroom supplies and solutions that lower maintenance costs and nearly eliminate downtime. Discover the trusted brands we work with to help you build the perfect cleanroom.
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cGMP Peptides Synthesis Services Manufacturers,Custom Cyclic Peptides and Branched Peptides companies,Custom Peptides Synthesis companies-3days delivery Online Sale,Custom Stable Isotope-Labeled Peptides,HIV Related Peptides Manufacturers
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cGmp Contract Manufacturing - AbbVie Contract Manufacturing AbbVie Contract Manufacturing has a track record of successful small molecule and biologics development, giving your project a strategic head start.
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PCD Pharma Company in Chandigarh | PCD C&F Pharma | Biocell Pharma Biocell Franchise Pharmaceuticals Pvt. Ltd. is a recognized pharma company in India. Company is dealing in Pharma Franchise, Pharma pcd, Pcd Pharma, Monopoly Pharma Franchise, Pharma pcd in baddi. due to our ability to manufacture, export and supply a diverse and qualitative range of Allopathic/Ayurvedic Medicines. Moreover, our range comprises Tablets, Capsules, Syrups, Injectables and many others.
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FinVector FinVector is a world leader in the research and development of Viral-Based Gene Therapy products, with state-of-the-art facilities and a highly experienced scientific team working in the gene therapy market.
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cGmp Contract Manufacturing - AbbVie Contract Manufacturing AbbVie Contract Manufacturing has a track record of successful small molecule and biologics development, giving your project a strategic head start.
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FinVector FinVector is a world leader in the research and development of Viral-Based Gene Therapy products, with state-of-the-art facilities and a highly experienced scientific team working in the gene therapy market.
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CGMP KGMP MCG경영컨설팅 ISO22716,EFfCI,화장품GMP,ISO13485,의료기기GMP,인허가,클린룸,적격성,밸리데이션
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cGMP Biologics Contract Manufacturing - CMO/CRO | MabPlex Mabplex provides world class biopharmaceutical & biologics contract manufacturing. One stop solution from early CRO to final CMO.
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cGMP Biologics Contract Manufacturing - CMO/CRO | MabPlex Mabplex provides world class biopharmaceutical & biologics contract manufacturing. One stop solution from early CRO to final CMO.
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Mebra - Producator de medicamente, pansamente si leucoplaste, cosmetice - Mebra MEBRA - producator de medicamente, pansamente, leucoplaste si cosmetice, producator al spray-ului Oximed. Game de cosmetice Mebra, Eritroacnol, Medara, Tonifor. Oximed este produsul de prima alegere pentru tratamentul arsurilor termice, arsurilor chimice, rani infectate, dermatite. Producator de medicamente certificat GMP , ISO 9001 si ISO 14 001
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FDA guidance, FDA compliance, FDA consulting, FDA regulations, FDA inspection, FDA guidelines, consultant compliance, Regulation Consulting, FDA information, FDA requirements FDA regulation compliance guidance services and consulting
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武汉纽斯特生物技术有限公司 武汉纽斯特生物技术有限公司官方网站
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Home - fdacompliancespecialists.com FDA Compliance Specialists, Inc. specializes in providing Global GxP, Medical Device, 21 CFR Part 11, and Supplier Quality Auditing, Computer System Validation, Inspection Readiness, and FDA Compliance and Quality Training Services to the Pharmaceutical, Medical Device, and Biotechnology regulated industries. The Quality of our services are best in class meaning we provide more benefits and value-added services for less money! Our cost-effective, highly credentialed FDA Compliance Specialists strengthen and improve the effectiveness of corporate internal and global supplier audit programs, computerized systems compliance, inspection readiness, and quality management system initiatives.
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PharmaVision - Home Located on a 50.000 m² campus in Topkapi/Istanbul, PharmaVision aspires to become a preferred partner in contract manufacturing to the pharmaceutical industry. The Company''s vision is in complete toll manufacturing partnership without any own licensing.
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CMC Drug Product Development Regulatory Consulting Pharma Pharmaceutical CMC regulatory consulting services - strategic planning, dossier preparation, training. RAC certified. Flexible/Professional/Effective.
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Contract Pharmaceutical Manufacturing, Process Development California Contract Manufacturer - 858-259-0969, Pharmaceutical manufacturing, clinical packaging, aseptic bottle tip cap filling, lyophilization services
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Contract Pharmaceutical Manufacturing, Process Development California Contract Manufacturer - 858-259-0969, Pharmaceutical manufacturing, clinical packaging, aseptic bottle tip cap filling, lyophilization services
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Exit AM Cleanroom Build & Performance performs cleanroom construction, cleanroom testing and certification, as well as cleanroom consulting services.
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CMC Drug Product Development Regulatory Consulting Pharma Pharmaceutical CMC regulatory consulting services - strategic planning, dossier preparation, training. RAC certified. Flexible/Professional/Effective.
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Contract Pharmaceutical Manufacturing, Process Development California Contract Manufacturer - 858-259-0969, Pharmaceutical manufacturing, clinical packaging, aseptic bottle tip cap filling, lyophilization services
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Laboratory Fine Chemicals & Culture Media Manufacturer & Exporters in India | CDH Fine Chemical CDH an ISO 9001:2008 & cGMP certified Manufacturer & Exporters of Laboratory Fine Chemicals, Laboratory Reagents & Dehydrated culture Media in India Since 1981. We provides Laboratory Fine chemicals & Culture Media for Microbiology in domestic & international market.
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Peregrine Pharmaceuticals is now Avid Bioservices • Avid Bioservices, Inc. Avid Bioservices, Commercial, Clinical, Biomanufacturing, manufacturing, biotechnology, biopharmaceutical, DNA manufacturing, virus manufacturing, protein manufacturing, microbial fermentation, mammalian, cell banking, contract manufacturing, CMO, biopharmaceuticals, cGMP manufacturing, GMP manufacturing
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Vitamins, Minerals, Bulk ingredients, Herbs, Vitamins Private Label, Custom Forumlas, Contract Manufacturer, Contract Packager AIE Pharmaceuticals is a full service contract manufacturer and packager of dietary supplements, functional foods, vitamins, minerals and herbal products
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Premium Supplements & Vitamins | Made in USA | GardaVita GardaVita provides premium nutrition with our dietary supplements and vitamins, all manufactured in a cGMP & FDA registered facility in Southern California
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Natural Wellness® - Natural Wellness For over 20 years, Natural Wellness supplements have been recommended by healthcare professionals and sold worldwide. All ingredients are of the highest quality and manufactured under the strict current Good Manufacturing Practice (cGMP) regulations ensuring all safety and quality standards are met.
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iPSC Banking Bank your own stem cells, generated using our proprietary induced pluripotent stem cell generation technology. Your cells are reprogrammed and cryo-preserved under FDA regulated cGMP conditions.
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HormoneSynergy® Online Store | Best Vitamins and Nutritional Supplements | Doctor Recommended Doctor recommended - HormoneSynergy the best vitamins and nutritional supplements manufactured in FDA registered and NSF inspected facilities certified cGMP
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Hercules Vitamins | Dietary Supplements Buying vitamins online couldn''t be easier! Browse Hercules Vitamins in New York and find the supplement that works best for your health or call 1-212-813-8000.
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Edge Pharmacy Services is a FDA certified compounding facility Edge Pharmacy Services is a Sterile and Non-Sterile compounding outsourced facility located in Colchester, Vermont. Our facility is maintained and operated in strict accordance with USP-797, USP-795, and cGMP guidelines. Our primary goal is to offer the highest quality compounded medications to hospitals, physicians, and patients. Please contact us for more information on our wide variety of preparations.
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HYY - Quality and Research Based Chinese Herbal Supplements HYY develops and distributes quality and research based Chinese herbal supplements for personal health. The herbal supplements are based on traditional principles yet manufactured under stringent cGMP standards.
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A&C manufacturer excipients process solutions buffers API A&C, your global GMP partner. Supplier of excipients, active pharmaceutical ingredients, process solutions, buffers, lab chemicals and solvents.
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细胞销售支持网- 亚洲干细胞️旗下“新生泉国际干细胞治疗医院”是首批获批入驻海南省博鳌乐城国际医疗旅游先行区、以世界先进水平的干细胞治疗技术为核心的干细胞专科医院。 亚洲干细胞️/新生泉国际干细胞治疗医院坚持“安全有效、科学基础、合规合法”和“客户利益高于一切”的原则,依托其中国目前唯一符合“中国CFDA/美国FDA/欧盟EMA国际cGMP/cGCP标准”的临床级细胞制剂独立大楼生产基地,遵照国务院海南先行区“先行先试”政策(国函[2013]33号),“一站式”提供干细胞保健与医疗综合服务,首批推出的项目包括干细胞抗衰、美容、卵巢修复、关节修复、男性生殖系统保健、肝脏功能保健、子宫内膜修复、改善类风湿症状、改善糖尿病症状等。 医院下设多个功能中心,包括细胞治疗中心、干细胞储存中心、功能医学检测中心、血液净化中心、营养调理中心、保健SPA中心、理疗康复中心、运动康复中心等,可提供个性化、精准化的生物医学综合服务。