Megafine Pharma audit report | Rephine

The following Rephine audit reports are available for Megafine Pharma (P) Ltd.:


  • Megafine Pharma (P) Ltd.

Example audit report

To get more information on audit reports by Rephine, please click the green button below to get contacted by Rephine!

 

What is a Megafine Pharma (P) Ltd. audit report?

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Here you can find the GMP Audit Report for Megafine Pharma (P) Ltd..

This audit report is accessible to other pharmaceutical companies, providing a detailed evaluation of Megafine Pharma (P) Ltd.'s compliance with industry standards and regulations. What makes this report stand out? It's a deep dive into the company's operations, spotlighting their stringent adherence to industry norms, evidenced by certifications like GMP, CEP, DMF.

An audit report in the pharmaceutical realm is more than a mere document; it's a mirror reflecting a company's commitment to regulatory compliance, quality control, and internal policies. This report isn't just a checklist – it's a narrative showcasing how Megafine Pharma (P) Ltd. aligns with the highest standards of Good Manufacturing Practices (GMP) and beyond. It doesn't just highlight compliance; it uncovers potential areas for enhancement, offering pathways for continuous improvement.

When do you need an audit report?

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Utilizing this report means it's no longer necessary to audit this supplier yourself. The availability of this report demonstrates Megafine Pharma (P) Ltd.'s commitment to transparency and adherence to quality standards. It serves as a valuable tool for businesses looking to partner with or procure services from Megafine Pharma (P) Ltd., ensuring a well-informed and secure decision-making process. For further details and to access the full Megafine Pharma (P) Ltd. GMP Audit Report contact us.

Pharmaoffer is dedicated to enhancing transparency and trust within the pharmaceutical industry, and this report is a key component of that mission. Would you like to learn more about it, click here and someone from the Rephine team will reach out to you.

How much does an audit report cost?

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The cost of a Good Manufacturing Practice (GMP) audit report can vary significantly based on several factors. Here's a general overview: 

  • Complexity of the Facility: The more complex the manufacturing processes and facilities, the more in-depth the audit will be, leading to higher costs.

  • Industry and Product Type: Certain industries, like pharmaceuticals, biotechnology, and food, have stringent GMP requirements, which can make audits more expensive due to the specialized knowledge and thoroughness required.

  • Location of the Facility: Geographical location can impact costs due to travel expenses for the auditors, local economic conditions, and regulatory variations.

  • Audit Duration: The length of time needed to complete the audit also plays a role. A larger facility or one with more complex processes may require more time to audit thoroughly.

  • Scope of the Audit: The specific requirements of the GMP audit (like whether it's for the entire organization or specific processes) can affect the price.

For a precise and detailed quotation that is specifically tailored to the Megafine Pharma (P) Ltd.’s facility and operational scope, we encourage you to contact Rephine directly.

Save time and resources by accessing internationally recognized GMP audit reports, conducted by highly qualified auditors worldwide.

Each report includes a CAPA plan when applicable and covers key quality aspects, ensuring compliance with major regulatory authorities (FDA, EMA, TGA, and more).

Rephine's reports help you qualify suppliers efficiently without the need for additional audits.

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Example audit report
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Megafine Pharma


Megafine, established in 1995, is a privately owned and professionally managed enterprise with it's corporate office in Mumbai and two multipurpose manufacturing sites at Vapi & Nashik in India, Vapi facility being successfully inspected by US-FDA and the Nashik facility is being approved by BGVFHH Germany (EMA EU-GMP), Japan PMDA, Health Canada, TGA Australia, COFEPRIS Mexico & Korea MFDS. Both the plants are also certified by WHO GMP, ISO 9001:2008, 14001:2004 & OHSAS 18001:2007 and have been audited by several Innovators and leading Generic companies from time to time.