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Horn Pharmaceutical Consulting - ASMF, Active Substance Master File, US-DMF, Drug Master File, Certificate of suitability, CEP, CTA ,Clinical Trial Application, IND, Investigational New Drug Application, CTD, Common Technical Document, European MAA, Marketing Authorization Application, NDA, New Drug Application / BLA, Biologic License Application, SPCs, Summary of Product Characteristics, clinical or nonclinical study protocols and reports, clinical or nonclinical summaries and overviews, quality overall summaries, QOS, CMC-documents, regulatory strategies, Authorities, EMEA, FDA, GMP, GCP, GLP, quality systems, SOPs, training, pharmaceutical, biotechnology, API ,Active Pharmaceutical Ingredient manufacturer, contract manufacturer, contract laboratory, SME, Small and Medium-sized Enterprise, medical device industry, advanced therapy industry, pre-submission, submission, pre-approval, approval, post-approval phase
HORN Pharmaceutical Consulting provides regulatory and business advice to companies from the pharmaceutical, biotechnology and medical device industries.
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A-Bio Pharma Pte Ltd
A-Bio Pharma Pte Ltd, Singapore is Asia's pioneering biologics contract GMP manufacturer of therapeutic proteins, monoclonal antibodies, and vaccines based on biotechnology, mammalian and insect cell culture and purification.
A-bio.com ~
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The Pharma Cup 2011
The Pharma Cup 2011 is the first European Pharma Football Tournament created to bring together the worlds of Sport and the Pharmaceutical industry while promoting the inter-relationships between companies and enjoying our most favorite sport; … Football
Thepharmacup.com ~
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