Our expert, for your product safety
When introducing a pharmaceutical product on the market even a minor error can negate years of research and development work. Our expert (meeting § 14 standards of the German Medicines Act), Dr. rer. nat. Herbert Geldermann, stands ready to assist in the optimization of your specifications, offer law-related pharmaceutical advice and to prepare and generate approval documentation for the marketing of your product. Dr. Geldermann looks back on many years of profound experience and takes his task of responsibility personally. You can rest assured that the registration process runs efficiently, smoothly and following Good Manufacturing Practice norms. At the end of the process, you will be left with a marketable product that meets all quality requirements.