Teva API audit report | Eurofins
The following Eurofins audit reports are available for Teva API:
Teva, Rho - Italy, Audited on site on 7 and 15/09/2021
Teva, Rho - Italy, Audited on site on 05/06/2024
Teva (Assia Chemical), Be?er Sheva - Israel, Audited on site on 05/12/2023
Teva, Sajobabony - Hungary, Audited on site on 17/10/2023
Teva, Opava - Czech Republic, Audited on site on 16/05/2023
Teva, Santhia' - Italy, Audited on site on 21/06/2022
Teva, Debrecen - Hungary, Audited on site on 31/05/2022
Teva, Gajraula - India, Audited on site on 10/05/2022
Teva, Debrecen - Hungary, Remote audited on 27/05/2021
Eurofins Healthcare Assurance
Eurofins Healthcare Assurance helps pharmaceutical/healthcare manufacturers to control their complex supply chains with Quality Assurance and GXP Auditing services. The Audit process is fully customized to meet the client’s needs.
The scope of our Auditing services covers:
GMP (Good Manufacturing Practice) & ISO: Finished Products, APIs and Excipients, Starting Materials, Cosmetic Ingredients and Products, MD Components, Food (Dietary) Supplements, Packaging Materials, Service Providers for Analytical Testing, Sterilization, Maintenance, Validation, Storage, Distribution.
GLP (Good Laboratory Practice): Laboratories used to perform all non-clinical safety studies which are intended to support research permits or marketing authorization.
GCP (Good Clinical Practice): Clinical Research Organization, Investigation Center and Data Center.
GVP (Good Pharmacovigilance Practices): SDEA, Pharmacovigilance systems and services.
Audit Reports
By purchasing our Audit reports, pharmaceutical companies can qualify their suppliers saving time and resources.
Our Audit report documentation is supported by a CAPA plan, when applicable. We can also provide additional documents and services when required.
Our Auditors are highly qualified and spread all over the world, and their CVs will be provided as well along with each Audit report.
Our Audit reports are well recognized by international authorities (ANVISA, COFEPRIS, EMA, FDA, HC, TGA, MHPRA, Swissmedic, etc.) and ready to be used for QP declarations.
Our GMP Pharma Audit report covers the main quality topics: Introduction, Follow-up of the previous Audit, Quality management, Organization and personnel, Documentation and records, Complaints – Recall, Deviations - Corrective Action & Preventive Action (CAPA), Product Quality Review (PQR), Audits, Rejection and Re-Use of Materials, Validation, Change Control, Suppliers and contract manufacturers (including laboratories), Quality Risk Management, Facility tour, Storage and Warehouse, Production and packaging areas, QC laboratories, Distribution, Conclusion.
What is a Teva API audit report?
Here you can find the GMP Audit Report for Teva API.
This audit report is accessible to other pharmaceutical companies, providing a detailed evaluation of Teva API'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 Teva API 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?
Utilizing this report means it's no longer necessary to audit this supplier yourself. The availability of this report demonstrates Teva API'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 Teva API, ensuring a well-informed and secure decision-making process. For further details and to access the full Teva API 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 Eurofins team will reach out to you.
How much does an audit report cost?
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 Teva API’s facility and operational scope, we encourage you to contact Eurofins directly.
Offers audits for industries as pharmaceutical, medical devices, cosmetic/personal care or food supplements.
GMP, GCP & GLP Audits
Additionally also internal audits programmes, Due Diligence Audits, GDPR audits
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