GMP Training
The individual elements of a quality assurance management system in the pharmaceutical industry are essential to ensure the efficacy and safety of drugs. National and international regulatory requirements must be met. The establishment and implementation of an effective quality assurance system also leads to more effective and efficient processes throughout the manufacturing chain.
Learn about the key processes of a pharmaceutical quality assurance management system and get up to date with regulatory requirements and industry trends.
GMP Consulting
Triggered by scientific and technological progress, more and more pharmaceutical companies find themselves in challenging situations. Navigating in a strictly regulated environment, with ever increasing requirements, such as in projects or in interaction with authorities, can bring great risks.
As experienced partners, we offer strategic support for specific short-term issues. Together with you, we plan the necessary steps to minimize potential risks.
GMP Project Work
Every company has to face various recurring challenges with limited resources. These resources can be knowledge, experience or simply the number of staff. It is not always possible to predict in the long term when and how a resource bottleneck will arise. We offer our customers a needs-oriented solution at short notice.
From the strategic planning of GMP projects, to the support of project activities, to the operational processing of work packages within a project, we offer a wide range of services.
GMP Trainings in detail
You need a GMP training for a specific topic? No matter if it is a basic training or an expert training, in the training center of TGMP Consulting you can choose between GMP basic trainings and expert trainings on the most important processes in the pharmaceutical quality management system. Choose the web based trainings on our platform and book them directly. Afterwards, you can play the training on your computer whenever you want, with as many interruptions as you like. Another alternative are our web based online seminars. Here you can interact with your instructor online on our training platform. In addition to the presentation, your instructor will help you to consolidate the topics learned directly in practical case studies in a workshop. Of course, you can also ask specific questions at any time and thus adapt the training to your needs.
Our virtual training center is currently under construction and will be available soon.
Consulting services in detail
Our second area of expertise is consulting in the pharmaceutical industry. Are you facing an important inspection, major challenges after an inspection or do you need a structured concept development for an important project or initiative, with a tight budget and schedule? We can support you with our knowledge and years of experience. Contact us conveniently through our online contact form and we will get back to you promptly. You can also call us directly.
TIMUR GÜVERCINCI
Trainer and consultant with more than 17 years of experience in the pharmaceutical and medical device industry. Management of various projects and organisations, with increasing responsibility. Fundamental “end-to-end knowledge” in processes and regulatory requirements from development to commercialisation of pharmaceuticals and medical devices. Experience in setting up and restructuring organisations. Freelance speaker and consultant for quality management topics in the pharmaceutical and medical device industry since 2016.
- Senior Director Head of Quality, Management Representative, Person Responsible for Regulatory Compliance – Multi Site Quality Organisation – Class IIb/II Medical Devices
- Director Head of External Supply Quality Processes and Development – Global Quality Assurance / Pharmaceutical Industry
- Director Head of Quality Assurance Chemical and Pharmaceutical Development / Pharmaceutical Industry
- Associate Director Head of Validation / Qualification and Engineering / Pharmaceutical Industry
- Quality Manager, Deputy Head of Quality Planning & Validation / Medical Device Industry
- Head of Validation / Pharmaceutical Industry
- Senior Project Engineer -/Service Provider for Pharmaceutical Industry
- Validation Engineer / Pharmaceutical Industry
WHITEPAPER
The application of artificial intelligence in the process validation of medicinal products in compliance with GMP requirements
Free Download
Service Offer
Service Package: Continued Process Verification Program for marketed medicinal products
Free Download
EMPLOYER AND BUSINESS PARTNER
CONTACT
Address
TGMP Consulting
Alteburgstrasse 51
72762 Reutlingen
Contact
info[at]tgmp-consulting.com
+49 172 5744280