Salinen Austria AG audit report | Eurofins

The following Eurofins audit reports are available for Salinen Austria AG:

Salinen, Ebensee - Austria, Audited on site on 21/06/2022

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 Salinen Austria AG audit report?

Here you can find the GMP Audit Report for Salinen Austria AG.

This audit report is accessible to other pharmaceutical companies, providing a detailed evaluation of Salinen Austria AG'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 Salinen Austria AG 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 Salinen Austria AG'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 Salinen Austria AG, ensuring a well-informed and secure decision-making process. For further details and to access the full Salinen Austria AG 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 Salinen Austria AG’s facility and operational scope, we encourage you to contact Eurofins directly.

Eurofins APIs on Pharmaoffer

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

Our services:

GMP Audit Services
Third party audits
GxP Consultancy
Quality Assurance
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Salinen Austria AG

Focus on specialty salts, it is taking a 7000-year-old tradition of salt mining in the Salzkammergut into the future.At locations in Altaussee, Hallstatt and Bad Ischl, over 4 million cubic meters of brine are generated annually, from which 1.2 million tons of salt are produced.Salinen Austria AG is a member company of the Österreichische Salinen Aktiengesellschaft, which also includes Salzwelten GmbH, Salinen Beteiligungs GmbH and Salinen Immobilien Gesellschaft m.b.H..


The quality of products from Salinen Austria AG is assured by means of a full spectrum of controls and inspections. The entire analysis process, from raw natural resources to finished product, is part of a quality-assurance chain that utilizes state-of-the-art methods in our own accredited laboratories. Systemized traceability allows for comprehensive audit- and supplier management. The safety of products and production methods is inspected systematically by means of a HACCP quality-management approach, thereby guaranteeing optimal quality.

Pharmaceutical Salt as Active Pharmaceutical Ingredient

Highest standard for pharmaceutical products requiring the highest purity and GMP-certification.


Typical applications of PHARMASAL API are IV-solutions, injectables, parenteral dosage forms, peritoneal dialysis solutions, penicillin production, fractionation of blood plasma, applications in biopharma or as active pharmaceutical ingredient for various medical products. Furthermore PHARMASAL is also particularly suitable for cosmetics, skincare and wellness products, for inhalation in salt rooms and a variety of industrial applications requiring the highest purity.