Pharmaceutical Regulatory Affairs Services

Finished Products: Drugs / Herbal / Nutritional Supplements / OTC

Regcure Pharma India offers expert regulatory solutions to support accurate submissions using existing data and documentation. Our team ensures well-structured technical writing and streamlined submission processes for clients worldwide.

Our Regulatory Affairs Services Include:


1. Dossier Preparation & New Product Development

  • Preparation and submission of registration dossiers to global regulatory agencies in eCTD, CTD, and ACTD formats.
  • Assistance with administrative documents, submissions to Ministries of Health (MOH), and post-submission support including query resolution.

2. Active Substances: DMF / ASMF / CEP

We specialize in preparing Drug Master Files (DMF), Active Substance Master Files (ASMF), and Certificates of Suitability (CEP):

  • Evaluation and alignment of documents and data per international regulatory guidelines.
  • Customized support for open (applicant) and closed (restricted) parts of DMFs.
  • Preparation of EDMF / ASMF for CEP submissions to the European Union.

3. Clinical Services

Our clinical regulatory support spans the entire drug development journey:

  • Preclinical and clinical overviews through in-depth literature reviews and journal analysis.
  • Management and monitoring of clinical trials across therapeutic areas.
  • Support for:
    • Bioavailability (BA) and Bioequivalence (BE) studies
    • Clinical Trial Studies
    • Analytical solutions
    • Medical writing
    • Periodic Safety Update Reports (PSUR)
    • Risk Management Plans (RMP)
    • Toxicology studies (Carcinogenicity, Teratogenicity, Reproductive toxicity)
    • Therapeutic justifications for Fixed Dose Combinations (FDCs)

We help you ensure regulatory compliance, improve operational efficiency, and reduce costs.


4. Additional Services

  • Preparation of Summary of Product Characteristics (SmPC), Package Inserts, and Product Rationales
  • Analytical support for method development and validation
  • Routine product analysis using HPLC, GC, MS, UV, titration, and other techniques
  • Site Master File preparation
  • Dossier compilation per latest country-specific guidelines

Why Choose Regcure Pharma?

✅ Global Expertise
✅ End-to-End Regulatory Support
✅ Cost-Effective, Compliant Solutions

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