Laboratory
Heinrich Klenk GmbH & Co. KG is a corporate of the pharmaceutical industry. We are supervised and audited by the Government of Upper Bavaria located in Munich. Since 1996 we are audited according to GMP-Guidelines and are entitled to produce pharmaceutical goods according to the German pharmaceutical law (AMG § 13).
In our quality assurance manual we have laid down our quality policy. This manual is a ground manifest that grants the constant high quality of our products. An electronic version is available and can be requested at any time. Please send your e-mails to: robert.parzinger@klenk-herbline.de
Pharmaceutical liable persons:
Management: |
Heinrich Ludwig Klenk
Heinrich Klenk Junior
E-mail: heinrich.klenk@klenk-herbline.de | | | Chief of quality assurance:
Chief of production
Quality assurance manager
Information appointee and product-recall manager
Qualified person | Pharmacist Robert Parzinger
Tel.: +49 (0) 9723 / 609 41
Fax: +49 (0) 9723 / 609 35
E-mail: robert.parzinger@klenk-herbline.de | | | Chief of quality control |
Certified Biologist Dr. Gerald Binder
Tel.:+49 (0) 9723 / 609 39
Fax:+49 (0) 9723 / 609 35
E-mail: gerald.binder@klenk-herbline.de |
All goods in our product range are tested according to the latest pharmacopoeia in our own in-house laboratory. Drugs that are not mentioned in pharmaceutical pharmacopoeias are analysed according to the current, effective KLENK-specification.
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