Scientific Support Services

Ancla

Regulatory Medical Writing

  • Clinical Trial Protocol (CTP).
  • Informed Consent Form (ICF).
  • Journal/conference submission.
  • Investigator’s Brochure (IB) and Investigator’s Brochure update.
  • Clinical Study Report (CSR)/Clinical Trial Report (CTR).
  • Narratives.
  • Investigational New Drug Annual Report (INDAR).
  • Developmental Safety Update Report (DSUR).
  • Periodic Safety Update Report (PSUR)/ Periodic Benefit Risk Evaluation Report (PBRER).
  • Periodic Adverse Drug Experience Report (PADER).
  • Risk Management Plan (RMP)).
  • Risk Evaluation and Mitigation Strategy (REMS).
  • Clinical Overview.
  • Clinical Summary.
  • Nonclinical Overview.
  • Nonclinical Summary.
  • Addenda to Clinical Overview Reports.
  • Summary Bridging Reports.
  • Summary of Clinical Safety.
  • Summary of Clinical Efficacy.
  • Summary of Product Characteristics.
  • Pediatric Investigational Plan (PIPs).
  • Package Insert (PI).
  • Product Monograph.

  • Manuscript.
  • Abstract.
  • Poster.
  • Slide Deck.
  • Medical Information.
  • Literature Search.
  • Newsletter.

Medical Communications

Contact Us

India

Ancla Consultancy Services (India) Pvt. Ltd.Level 5, CR Towers, 100 Feet Rd VIP Hills, Silicon Valley, MadhapurHyderabad, Telangana 500081, India


Phone: 040-42000029

hello@anclacorp.com

United States

Ancla Consultancy Services LLC300 Carnegie Center Drive Suite 150 PrincetonNJ 08540 United States


Phone: 609-779-1600

hello@anclacorp.com