Pharmacovigilance

Evaluation of safety data

Serious adverse event/Death narratives

Serious adverse event (SAEs) data management

Writing of periodic safety reports (PSUR)

Quarterly and annual safety reports

Investigator brochures

Regulatory Affairs

Clinical Evaluation Reports

Pre-clinical expert reports

Clinical and pre-clinical overviews

Clinical summaries

Writing of standard operating procedures (SOPs)

Clinical Trials Design/Execution

Study protocols (Phase I-IV)

Case report forms (CRF)

Investigator brochures and annual updates

Informed consents

Applications to respective ethics committees

Study reports

Post marketing surveillance trials

Medical Writing/Communication

Congress services/reporting

Journal articles

Manuscripts for Peer-Review

Case reports

Abstracts

Posters

Slide decks

Literature reviews

Presentations

Brochures

Newsletters

Review articles

Editing

Proof reading

Publication planning