GMP Audit & Consulting Services

Product Description

We aim to provide the most reliable and preferred service platform to pharmaceutical companies worldwide for R&D cycleregulatory affairs, and GMP compliance with a higher benchmark of quality, integrity, and ethics.

As a Zenovel, we offer various GMP services which can help clients across the globe, ranging from audits to various consulting services. We provide the following comprehensive GMP Quality Compliance services to the pharmaceutical industry.

A.   GMP Audit Services:

 
✔ QMS Audit

✔  Vendor Qualification/Assessment Audit

✔  GAP Audit

✔  Pre-Inspection Audit

✔  Independent Supplier Audit (System & Facility Audit)

✔  Remote/Virtual Audits

✔  Regulatory Compliance Audit

Apart from this, we also provide the ready audit reports of different suppliers to our clients if available to us at a cost-effective rate which eliminates the process of going through the entire auditing process to get the supplier qualified/requalified.


B.    GMP Consulting Services:


✔  Designing of Procedures and SOPs, WI, Policies, Forms, Formats,

✔  GAP Review of Quality System and Support in Improving the Documentation System

✔  Root Cause Investigation

✔  OOS Procedure Optimisation, Change Control, Training

✔  Outsourcing Management with Resource Optimisation and Quality output in a time-bound manner.

✔  CAPA Plan and Management

✔  Plant Set up and Upgradation

Zenovel

  • IN
  • 2021
    On CPHI since
  • 1
    Certificates
  • 25 - 49
    Employees
Company types
Consultancy
Contract Service
Primary activities
Clinical Research
Medical Devices
Other
Regulatory Affairs
Specifications
  • Selling Points
    Brand Name; Convenience; Experienced Technicians; Guarantee/Warranty; International Approvals/Standards; Product Performance; Quality Service; Reputation
  • Model
    Good Manufacturing Practices

Zenovel

  • IN
  • 2021
    On CPHI since
  • 1
    Certificates
  • 25 - 49
    Employees
Company types
Consultancy
Contract Service
Primary activities
Clinical Research
Medical Devices
Other
Regulatory Affairs

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