Our Experts

Mentors & Regulatory Professionals

IMEX Consultancy Services is backed by a team of seasoned regulatory professionals with decades of hands-on experience across pharmaceuticals, cosmetics, medical devices, food regulations, and clinical research.

Mr. Rajesh Patel

Senior Regulatory Affairs Consultant

Drug Manufacturing Licenses · GMP / Schedule M · CDSCO

20+ Years

A seasoned pharmaceutical regulatory professional with over two decades of experience in drug manufacturing licensing, GMP compliance, and CDSCO submissions. Has guided 200+ pharmaceutical units through facility setup, Schedule M compliance, and regulatory inspections across Gujarat, Maharashtra, and Rajasthan.

Areas of Expertise

Drug Manufacturing LicensesRevised Schedule MGMP AuditsFDCA / CDSCO LiaisonSMF & Quality ManualsValidation Protocols

Ms. Priya Sharma

Cosmetics & Medical Device Regulatory Expert

Cosmetics Rules, 2020 · Medical Devices Rules, 2017 · CDSCO Import

15+ Years

Specialist in cosmetic product licensing and medical device regulatory affairs. Extensive experience in CDSCO import registrations, Cosmetics Rules 2020 compliance, and Class A–D medical device licensing. Has supported domestic and international brands in navigating India's evolving cosmetic and device regulatory landscape.

Areas of Expertise

Cosmetic Manufacturing LicensesImport Registration (CDSCO)Medical Device Class A–DISO 13485 QMSLabeling ComplianceRegulatory Dossiers

Mr. Suresh Mehta

Food & Nutraceutical Regulatory Advisor

FSSAI · Food Supplements · Health Products

18+ Years

Expert in FSSAI licensing, food supplement regulatory frameworks, and nutraceutical product compliance. Has assisted food manufacturers, importers, and health supplement brands in obtaining FSSAI approvals, product registrations, and compliance documentation across India.

Areas of Expertise

FSSAI LicensingFood Supplement ComplianceNutraceutical RegulationsHealth Product ApprovalsLabeling & ClaimsState Food Authority Liaison

Mr. Anand Verma

Legal & Enforcement Compliance Specialist

Drugs & Cosmetics Act · NDPS Act · Court Matter Support

22+ Years

A highly experienced regulatory compliance specialist with deep expertise in the Drugs & Cosmetics Act, 1940, NDPS Act, 1985, and enforcement matters. Has provided technical and legal documentation support in regulatory proceedings, NSQ drug investigations, and Risk-Based Inspection preparedness for pharmaceutical companies across India.

Areas of Expertise

Drugs & Cosmetics Act ComplianceNDPS Act Regulatory SupportCourt Matter DocumentationNSQ Drug InvestigationsRBI ReadinessCAPA Development

Dr. Meena Iyer

Clinical Research & Stability Study Expert

Clinical Trials · GCP · ICH Stability Guidelines · SMO

16+ Years

Clinical research professional with extensive experience in clinical trial management, Site Management Organization (SMO) operations, and stability study design. Specialises in GCP compliance, BA/BE study coordination, pharmacovigilance, and ICH/WHO stability protocols for pharmaceutical and nutraceutical products.

Areas of Expertise

Clinical Trial ManagementGCP ComplianceBA / BE StudiesStability Study ProtocolsPharmacovigilanceEthics Committee Submissions

Mr. Vikram Joshi

Quality Assurance & Testing Laboratory Consultant

NABL Labs · IP/BP/USP Testing · GMP Quality Systems

17+ Years

Quality assurance expert with a strong background in pharmaceutical testing, NABL-accredited laboratory coordination, and quality management systems. Has supported manufacturers in raw material testing, finished product release, stability studies, and method validation across drug, food, and cosmetic categories.

Areas of Expertise

Pharmaceutical Testing (IP/BP/USP)NABL Lab CoordinationStability TestingMethod ValidationQuality Management SystemsCOA Review & Compliance

Work with India's Leading Regulatory Experts

Our mentors bring decades of combined experience to every client engagement — ensuring your regulatory journey is smooth, compliant, and cost-effective.

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