WHY CHOOSE US

Faster, Value-Driven Approvals

Always aspires to provide efficient and value-added support in obtaining faster Regulatory approvals for our clients.

Global Regulatory Leadership

A Top-of-mind company in the global Regulatory Services.

Empowering Client Growth

Dedicated to growth of client, boost agility and widen the chances of regulatory approval for the pharmaceutical companies

About Us

VRS Healthcare is dedicated to delivering reliable and compassionate healthcare services that support patients and families with their medical needs

End-to-End Compliance

VRS Healthcare is end-to-end Regulatory Service capabilities has helped us ensure full compliance to regulatory guidelines and timelines.

Safety-Driven Partnership

VRS healthcare is committed to improving health in partnership with its clients. We bring together safety, medical, regulatory and technology resources to ensure that patients receive the safest, most effective therapies possible.

Global Regulatory Expertise

VRS healthcare is an India-based regulatory services company started in 2020 by an experienced professional team. Today, we are provide as a global regulatory services with more than 120+ Clients.

Our Services

Regulatory Services

  • Regulatory Dossier filling for;Dossier technical review and e-ctd submission and publishing with software for regulated market and Dossier Preparation, Technical Review and Compilation (CTD, ACTD, Country Specific or Regional Submission) for ASEAN, CIS, AFRICA, GCC and many ROW markets.
  • Dossier Preparation for Nutra, veterinary & Herbal Product. Query Response of submitted submissions.
  • Drug Master file (DMF)
  • Analytical Method Validation for Dissolution, Assay, Related Substances (Impurity) and Residual Solvent. (HPLCwith chromatogram, UV- with spectrum) & Micro.
  • Comparative Dissolution Profile (CDP), (HPLC- with chromatogram, UV- with spectrum).
  • BA/BE report and Clinical Trial Report (CT). (Bio- analytical Validation / Report and Protocol)
  • Preparation of Product development rational, Process validation protocol/Report with Raw data calculation and statistical data, Stability data along with Chromatogram each time points, container closure integrity.
  • Global Labelling and Artwork
  • Patient Safety Update Report (PSUR), Risk management Plan (RMP) and Pharmacovigilance System Master File (PSMF), Standard Operating procedure For Pharmacovigilance Surveillance.
  • Global Language Translation
  • Legalization of document with all Embassy & Apostile.

Who- GMP Audit compliance services

  • Our GMP Audit Compliance Services ensure that your business meets the highest standards for Good Manufacturing Practices (GMP).
  • We offer comprehensive audits, assessments, and consultancy to help companies in regulated industries (pharmaceuticals, food, cosmetics, etc.) comply with GMP requirements.
  • Our services focus on identifying gaps in your processes, recommending corrective actions, and ensuring that your operations align with local and international regulatory standards.
  • We help you maintain product quality, safety, and compliance, reducing risks and ensuring smooth regulatory approvals.
300 +
Successful Dossier Submissions
98 %
Compliance Success Rate
12 +
GMP/PICS Audits Completed
120 +
Pharma Clients Served

Get in touch

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VRS Healthcare

We’d love to hear from you! Whether you have questions, need more information about our services, or are looking for personalized healthcare solutions, feel free to reach out.
Our team is dedicated to providing prompt and helpful responses. Simply fill out the form on the right or contact us directly through the details below.



Contact Us

613, Saffron Buisness park
Jasodanagar Ahmedabad 382445,
Gujarat, India
+91 9033968857
+91 9033825317
sweta_shah@vrshealthcare.in
ronak_shah@vrshealthcare.in