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Biomedical Consulting International Regulatory Submissions Medical Writing Risk Management Pharmacovigilance

Biomedical Consulting International, Inc. (BCI) is a global regulatory center for excellence with office locations around the world offering a one stop shop for all of your regulatory and dossier submission needs.

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Biomedical Consulting International Regulatory Submissions Medical Writing Risk Management Pharmacovigilance | biomedconsult.com Reviews
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Biomedical Consulting International, Inc. (BCI) is a global regulatory center for excellence with office locations around the world offering a one stop shop for all of your regulatory and dossier submission needs.
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Biomedical Consulting International Regulatory Submissions Medical Writing Risk Management Pharmacovigilance | biomedconsult.com Reviews

https://biomedconsult.com

Biomedical Consulting International, Inc. (BCI) is a global regulatory center for excellence with office locations around the world offering a one stop shop for all of your regulatory and dossier submission needs.

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Biomedical Consulting International

http://www.biomedconsult.com/ppb.html

Medical / Regulatory Writing. Medical / Regulatory Writing. Medical / Regulatory Writing. Medical / Regulatory Writing. Phase II Services - Pharmacology and Toxicology Consulting. BCI will either develop or assist the client to develop Pharmacology/Toxicology programs that are fully integrated with the clinical and regulatory drug development program.

2

Biomedical Consulting International

http://www.biomedconsult.com/rspa.html

Medical / Regulatory Writing. Medical / Regulatory Writing. Medical / Regulatory Writing. Medical / Regulatory Writing. Phase I Services - Regulatory Submissions. Abbreviated new drug applications (ANDA). Biologics license applications (BLA). Clinical trial authorization/application/exemptions (CTA/CTX). Clinical trial notifications (CTN). Common technical document (CTD). Drug master files (DMF). Investigational drug exemptions (IDE). Investigational new drug applications (IND). New drug submissions (NDS).

3

Biomedical Consulting International

http://www.biomedconsult.com/spb.html

Medical / Regulatory Writing. Medical / Regulatory Writing. Medical / Regulatory Writing. Medical / Regulatory Writing. Phase II Services - Safety and Pharmacovigilance. BCI offers safety and pharmacovigilance services to assist in the development of new drugs, biological and medical devices, as well as in all phases of clinical research.

4

Biomedical Consulting International

http://www.biomedconsult.com/rspb.html

Medical / Regulatory Writing. Medical / Regulatory Writing. Medical / Regulatory Writing. Medical / Regulatory Writing. Phase II Services - Regulatory Submissions. Abbreviated new drug applications (ANDA). Biologics license applications (BLA). Clinical trial authorization/application/exemptions (CTA/CTX). Clinical trial notifications (CTN). Common technical document (CTD). Drug master files (DMF). Investigational drug exemptions (IDE). Investigational new drug applications (IND).

5

Biomedical Consulting International

http://www.biomedconsult.com/cpa.html

Medical / Regulatory Writing. Medical / Regulatory Writing. Medical / Regulatory Writing. Medical / Regulatory Writing. Phase I Services - Chemistry, Manufacturing and Controls Consulting. BCI will either develop or assist the client to develop CMC programs that are fully integrated with the clinical and regulatory drug development program.

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