MEDATEQ LABS Consultants, we offer comprehensive Pharma Regulatory Support services to help pharmaceutical, biotechnology, Nutraceutical, Herbals, Intermediate and medical device companies meet international regulatory requirements efficiently and our experts provide end-to-end manufacturing to regulatory support across the entire product lifecycle.
Regulatory Affairs Service
Audit Outsourcing
GAP Analysis
Turnkey Project
New Product Manufacturing
Resources
MEDATEQ LABS regulatory team can assist with all of your pharmaceutical regulatory affairs needs, supporting your product lifecycle.We provide Comprehensive Solution for Preparation, Filing and Registration & Updates of Drug Master Files (DMF) for API
& Registration Dossiers for Formulations at a single contact point.
Regulatory Services:
Global Pharmaceutical Regulatory Affairs Services
Dossier Services
DCGI- Indian FDA
DMF Services
CMC Regulatory Support
Regulatory Medical Writing
Regulatory Submissions
Regulatory Submission Support
Regulatory Strategy and Lifecycle Support
MEDATEQ LABS provides support in developing complete documentation such as Quality Policy, Quality Manual & Objectives, Site Master File, Procedures, Specifications, Drugs Master File, SOPs, STPs, Guidelines, Environment Monitoring, Drawings, Flow Charts, BMRs, Formats & Data Sheets. Documentation also includes Document Distribution & Control, Review System, Change Control System, Recall, Complaint Handling, Non-Compliance & Non-Conformities.
GMP Compliance Services:
Quality Management and GMP Compliance Services
GMP Documentation
Audit Outsourcing
Client-Site Training
MEDATEQ LABS Pharma Consultants & GMP Services, we specialize in delivering end-to-end Turnkey Pharma Projects tailored for the dynamic needs of pharmaceutical, biotech, and healthcare sectors. Set up or upgrade pharma facilities with turnkey services—planning, design, construction, validation, and handover. we offer seamless, compliant, and cost-effective execution from concept to commissioning.
Turnkey Project:
Pharma turnkey projects Planning & Feasibility Study
Operational Support
Quality Management Systems Support
Regulatory Compliance Support
Licensing Support
Design & Engineering Support
Construction & Installation Support
Technology Transfer Support
MEDATEQ LABS have come up with new vertical of developing the source of pharmaceutical materials (APIs, Intermediates and starting materials).
Process Development Service
Technology Transfer
Pharma Formulation
Parenteral
Oral Solids Dosage
Topicals
MDI/DPI
