Special Feature

About the Company 

Amreteck® is a USA based worldwide Quality, Validation & GxP Compliance Consultancy Company, provides services to the Pharmaceuticals, Medical Devices and Biotech companies, incorporated in 2006, has been performing projects globally over several years.

Our strategy and strength are to help companies in Technical Services, Quality Management Systems, Validation, Project Management, Quality Assurance, Clinical and GxP (GMP, GCP, GLP) Compliance. Amreteck brings USA Pharmaceuticals Professional knowledge, experience and US-FDA Inspections expertise to you.

Amreteck® is organized into three primary Business Units:

PROFESSIONAL SERVICES - Engineering Quality Design Review, Clinical Trials Auditing, Commissioning & Validation, GMP, GCP, GLP Audits, Gap Assessment, Remediation, 483 Responses, Warning Letter Responses, Consent Decree Support, Risk Assesment, QA Oversight, QA Review & Approval, Quality Management Systems, Pre-approval Inspections (PAI) preparation, Start-up of Drugs Manufacturing Facilities, Technical Transfer, Scale-up, Cleaning Validation, Process Validation, Computer Validation, Process Development, Shipping Validation, Change Control Program, Calibration & Maintenance Programs, CAPA, Deviations, Master Validation Plan (MVP), Validation Project Plan (VPP), SOPs, Protocols Development & Execution, Development & Implementation of Validation, Quality Assurance & Audits Departments and Policies.

PHARMACEUTICALS ONLINE TRAINING - Amreteck offers various Pharmaceuticals Courses to train students to be prerpared for the career in the Pharmaceuticals Industries, enhance Pharmaceuticals Professionals job knowledge, experience & expertise to meet the global pharmaceuticals standards and expectation.

PHARMACEUTICALS INVESTMENT SERVICES - Perform companies's Quality & Operational Assessment to make decision on the investment opportunity.
Recent News

Amreteck® USA offers Online Training for the following Pharmaceuticals courses:

  • Pharmaceuticals - 101

  • Validation - 101

  • Validation - 201

  • Validation - 301

  • Quality Assurance - 101

  • Quality Assurance - 201

  • Audit/Compliance - 101

  • GMP - 101

  • GMP - 201