Services

Writing of all documents related to clinical studies (PhaseI-IV), including but not limited to the following:

Study Protocols and Amendments

Subject Information and Consent Forms

Clinical Study Reports

Investigator Brochures

Common Technical Documents

Subject Narratives

Compilation of Trial Appendices

Clinical Trial Registrations

EUDRACT Applications

Summaries of Product Characteristics

Manuscript Preparation and Editing

Abstracts and Posters

Literature Reviews

Product Monographs

Standard Operating Procedures

Document Standards and Templates

Style Guides

Training Manuals

Quality Control and Review of existing documents

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