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Contract Services

1 CRO and Regulatory Affairs Services in Turkey
R&D Company From Turkey can support regulatory affairs, tecnology trasnfer and  registration services in TurkeyAlso offering contract R&D service is available and license-out  of formulation documentation without clincal studies.  Please contactus for more details.  
1 Contract Manufacturer for Transderamal Drug Delivery System
Member of  Farmavita:net is looking for contract manufacture of product in form of Transdermal Delivery System.  Manufacturer must have EU GMP certificate.  Estimated annual purchase is 5 to 10 million pflasters.   Vendor also expect that manufacturer will provide some formulation development support, as well as do all necessary validations related to manufacture and QC.   

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KRAOGENPHARMA CONSULTANT N KAMALAKAR RAO M.Pharm.                                      raonk5@gmail.com                 Contact No. +91 9502592310 Generic Pharmaceutical...
Sodium Cromoglycate Eye Drops
Looking to develop sodium cromoglycate eye drops in 5,10 and 15ml multidose plastic bottle. Looking to market the product in UK and USA.
GxP audits-Key Starting Materials qualification-Regulatory services
GxP audits (GMP,GDP, GLP, GCP,etc.), facility feasibility audits, GAP analysis audits, supply security audits,computer system validations and CVS audits, GxP training
Regulatory affairs, CEP Application, registration services in EU and MENA, Technical transfers
Dossier comiplation, dossier review, dossier submission, registration services in EU and MENA, Pharmacovigilance, product development, tech transfers and scale-ups, facility design and upgrading
GDP certification

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GCP Certification of any facility (port, airport, railway station, truck/ vessel / plane transport company, warehouse, transportation means, etc.)

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