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Innovations and highlights in the Pharma industry 

Dive deep into the world of Pharma with Zamann’s Expert Blog. Our industry-leading professionals share insights on global project management, quality consultancy, digitalization, and more. Stay updated with trends and innovations transforming the Pharma industry. 

IQ, OQ, PQ: Essential Steps for Equipment Qualification

Equipment quality in pharmaceutical manufacturing is ensured through IQ, OQ, and PQ phases, validating installation, performance, and user needs. Regulatory mandates prevent hazards, like mislabeling, with ongoing compliance via requalification. Expert guidance streamlines validation efforts for robust, compliant systems.

What is GAMP 5 Guideline? Checklist for GAMP 5 compliance

GAMP is the acronym used to summarize the term “Good Automated Manufacturing Practices“. These are a compilation of recommendations published by the International Society for Pharmaceutical Engineering (ISPE) in the form of a book to provide guidance on the compliance of computerized systems in regulated industries.

Unveiling GMP Inspections: Key Deficiencies and Guidelines

In the pharmaceutical industry, GMP inspections ensure quality and compliance, demonstrating commitment to safety and building trust with healthcare professionals and patients. Understanding the inspection process, guidelines, and common deficiencies is crucial for upholding industry standards and ensuring patient safety.

News and more

Remote Patient Monitoring is not just a technology—it’s a paradigm shift in healthcare delivery. It empowers patients with more control over their health while providing healthcare providers with the data they need for timely interventions. As adoption grows, RPM promises
The landscape of drug pricing in the United States is currently undergoing a period of significant and unprecedented change, marked by potentially transformative reforms. This blog post delves into the intricacies of several key initiatives that are reshaping the pharmaceutical
The healthcare industry is embracing medical device sustainability through innovative materials and processes, aiming to reduce environmental impact while maintaining patient care standards.
Marketing in Pharma and Medtech is challenging—but rewarding. With the right training from Pharmuni, professionals can become trusted voices in healthcare, shaping responsible messages that support both commercial success and patient well-being.
To master laboratory method validation, understand key concepts like accuracy and precision, adhere to regulatory guidelines, and draft a comprehensive validation plan. Utilize statistical tools, document meticulously, and engage in continuous improvement. Collaborate with cross-functional teams and stay updated on
Audit trail gaps are among the top data integrity concerns during regulatory inspections. This article explores common pitfalls and how to avoid them with smart validation and QA practices.
Isolators and RABS both play critical roles in modern aseptic manufacturing, but their regulatory expectations differ significantly. FDA, EU, and ISO guidelines emphasize risk-based design, validated control measures, and procedural discipline.
Pharmaceutical firms must prioritize data integrity and robust procedures to meet FDA and EU regulatory expectations. Understanding their detailed guidelines is vital for compliance and data quality. Successfully navigating these regulations requires mastering FDA and EU requirements, including best practices