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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, qualit
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-doc
HORN Pharmaceutical Consulting provides regulatory and business advice to companies from the pharmaceutical, biotechnology and medical device industries.
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company.html | Company |
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quality_cmc.html | QOS |
clinical_development.html | clinical |
due_diligence.html | Review of product development status, evaluation of development strategies, preparation of due diligence reports [more] |
regulatory_affairs_training.html | Training for Regulatory Affairs, GMP, GCP, GLP; in-house training specifically tailored to your needs [more] |
regulatory_intelligence.html | Regulatory intelligence focuses on the essentials in the regulatory world [more] |
non_clinical_development.html | nonclinical |
quality_CMC.html | CMC |
gmp.html | GMP |
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