Karl Metzger is Managing Partner, CEO of gmPlan with focus on both GMP and GDP, auditing & consulting. The Chemist acts as Qualified Person according to § 14 AMG as well as certified Auditor. Since more than 20 years he is conducting audits and managing GMP-Projects – worldwide.
Dr. Ekaterina Biehlig is responsible for quality relevant questions in the GDP & GMP area. She also focuses on quality control and training. As graduated material scientist, Dr. Biehlig got her PhD title in the polymer chemistry and physics field. She gained her experience as application chemist in an analytical instrumentation producing company.
Dr. Christian Hauck is a pharmacist, who has been working in this field for more than 30 years. His profound knowledge stems from his experience as a Qualified Person, head of production, pharmaco-vigilance manager, information officer, and responsible person for wholesale and is highly beneficial for the GMP auditing, GMP office & training.
With a Diploma in pharmaceutical studies and a specialization on pharmaceutical analytics, Dr. Wolfgang Heisig worked for more than 30 years in the fields of quality control and quality assurance. He is the gmPlan expert for GMP auditing, consulting and training and is a Qualified Person in accordance with the (German) law.
Dr. Volker Kukla has spent his entire professional career in the international medical technology segment. As product manager, research and production manager, he gained experience from different perspectives with the European and American approval regulations. He supports gmPlan in ISO9001: 2015 and ISO13485 issues for medical devices and the FDA requirements.
The physician Hans Metzger is Head of Medical Science and part of our Pharmacovigilance team. Besides his activities for gmPlan, he has been working as anesthesiologist in a hospital and as emergency physician for many years.
Carolina Schulte is concerned with quality and hygiene management, as well as with quality control in the fields of GMP consulting & training. In addition, as a graduate microbiologist, she is in charge of Pharmacovigilance. She gained her expertise in a GMP/GLP contract laboratory and in an interface function for customer concerns and quality management matters in a globally operating corporation.
After earning a degree in media and communication studies with the main focus on advertising, she gained professional experience in renowned international agencies. Following 17 years in the world of advertising Josefina started anew as the managing director´s assistant at gmPlan. She is also responsible for the marketing department, ensures that the seminars run smoothly and is often the initial contact for our clients.
Dr. Maina Wehner focuses on the area of regulatory affairs and manages authorization procedures for medicinal products and active substances on national and international markets. After her postgradual degree in Drug Regulatory Affairs the veterinarian worked in a regulatory affairs department of a pharmaceutical company in northern Germany.
Doria Zuo is Project Manager and represents gmPlan in China. Besides establishing our office in Chongqing, her focus is on GMP training & auditing. After graduating in biological engineering she gained her knowledge and experience of quality control and pharmaceutical quality management by heading the QC department of a pharmaceutical company for more than six years.