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Global Regulatory Affairs & Healthcare Training Solutions

Navigating Compliance. Empowering Excellence.

Helping pharmaceutical, nutraceutical, medical device, and healthcare organizations achieve regulatory compliance, market access, and professional excellence through expert advisory and industry-focused training.

  • Product registration & dossier preparation
  • Medical affairs & scientific writing
  • Pharmacovigilance & clinical research
  • Regulatory, GCP & healthcare training
  • Donor-funded public health programs
  • USFDA
  • DRAP
  • Health Canada
  • CE Mark
  • ICH-GCP
  • Pharmacovigilance
Dr. Mohammad Zakir, founder of MedReg Advisory Services

Founder Profile

Dr. Mohammad Zakir

MBBS | Clinical Research Professional | Regulatory Affairs & Healthcare Training Expert

Dr. Mohammad Zakir is a senior healthcare and pharmaceutical professional with expertise in regulatory affairs, medical affairs, pharmacovigilance, clinical research support, and healthcare training. He has successfully managed international regulatory projects, healthcare training initiatives, and donor-funded public health programs across Pakistan and international markets.

25+
Years Experience
4
Regulatory Jurisdictions
Pharma
Devices & Public Health

About Us

Who We Are

MedReg Advisory Services is a healthcare consulting and training firm specializing in regulatory affairs, medical affairs, clinical research support, pharmacovigilance, and healthcare capacity building.

We combine scientific expertise, regulatory knowledge, and training excellence to help organizations navigate complex compliance environments while strengthening healthcare systems and workforce capabilities.

What We Do

Our Services

Regulatory Affairs & Compliance

Achieving regulatory approvals and maintaining compliance across local and international markets.

  • USFDA Regulatory Guidance
  • DRAP Product Registration Support
  • CTD/eCTD Dossier Preparation
  • Medical Device Regulatory Support
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  • Nutraceutical & Dietary Supplement Registration
  • CE Mark Documentation Support
  • Technical File Preparation
  • Labeling & Artwork Compliance
  • GMP & Regulatory Compliance Advisory
  • Regulatory Gap Assessments
  • Product Lifecycle Management

Medical Affairs & Scientific Support

Scientific expertise supporting product development, compliance, and healthcare engagement.

  • Medical & Scientific Writing
  • Clinical Literature Review
  • Medical Review of Promotional Materials
  • Pharmacovigilance Support
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  • Product Monographs & Scientific Content
  • Medical Training Programs
  • Scientific Presentations & Workshops
  • Healthcare Provider Education

Clinical Research & Pharmacovigilance

Support for clinical and post-marketing research activities.

  • Clinical Trial Protocol Development
  • ICH-GCP Compliance Support
  • Pharmacovigilance System Development
  • Adverse Event Reporting Frameworks
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  • Seeding & Observational Study Support
  • Clinical Documentation Review
  • Research Coordination & Monitoring

Training & Capacity Building

Professional training programs for healthcare and pharmaceutical professionals.

  • USFDA & DRAP Regulatory Affairs
  • Pharmacovigilance & Drug Safety
  • Clinical Research & GCP
  • Medical Writing
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  • Healthcare Communication Skills
  • Sales Force Scientific Training
  • Quality & Compliance Training
  • Healthcare Provider Capacity Building
  • Public Health Program Training

Public Health & Development Consulting

Technical and strategic support for donor-funded health initiatives.

  • Program Design & Proposal Development
  • Monitoring & Evaluation Frameworks
  • Healthcare Workforce Training
  • Health Systems Strengthening
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  • Stakeholder Engagement
  • Donor Reporting & Compliance
  • Public Health Strategy Development

Delivery Formats

How We Deliver Training

  • In-Person Workshops
  • Virtual Training Programs
  • Customized Corporate Training
  • Training of Trainers (TOT) Programs

Why Choose Us

Why MedReg Advisory Services

Extensive Industry Experience

25+ years across pharmaceuticals, healthcare, clinical research, and public health.

International Regulatory Exposure

USFDA, Health Canada, DRAP Pakistan, CE Mark, and other international authorities.

Practical & Customized Solutions

Consulting and training aligned to organizational goals and compliance requirements.

Cross-Sector Expertise

Pharmaceuticals, medical devices, nutraceuticals, clinical research, and public health programs.

Capacity Building Focus

Proven track record training healthcare professionals, regulatory teams, and field staff.

Who We Work With

Industries We Serve

  • Pharmaceutical Companies
  • Nutraceutical & Dietary Supplement Companies
  • Medical Device Companies
  • CROs & Clinical Research Organizations
  • Healthcare Institutions
  • NGOs & Development Organizations
  • Healthcare Startups
  • Regulatory & Compliance Teams

Ready to Strengthen Compliance and Build Healthcare Excellence?

Partner with MedReg Advisory Services for expert regulatory guidance, healthcare training, and scientific consulting solutions.

Contact Us Today

Enquiries are answered directly by Dr. Zakir. If your question concerns an active submission or an audit deadline, say so in the message and it will be prioritised.

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