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As a Head of Regulatory Affairs & Clinical Operations operates internationally with flexible business models and fully, ICH-GCP -trained operational staff and personnel trained on Regulatory Affairs Guidelines and Procedures.
RegPharmaClin can provide you with a proficient and well-trained Clinical Operations staff to ensure the highest quality standards of the services offered.
RegPharmaClin can provide you with an extensive network of experienced and ICH GCP R2 trained CRAs operating on pan-European level.
Clinical trial execution is closely monitored by a dedicated team with the responsibility to process real-time information on study progress.
Strategically selecting the right sites to conduct clinical trials is essential to ensure the success of a trial with the therapeutic specific site knowledge of RegPharmaClin.
The pharmaceutical industry continually faces increased focus and inspections by health authorities, coupled with travel restrictions and complex globalised supply networks.
If you want to better understand the latest trends and developments and put new knowledge into practice, contact RegPharmaClin.
A Head of Regulatory Affairs & Clinical Operations, Leading Expert on Regulatory Affairs & Drug Development with over 31 years pharmaceutical experience. Provides a full range of services and therapeutic areas including Regulatory Medicinal Products, Biological Medicinal Products, Veterinary Medicinal Products, Generics, OTCs, Medical Devices, Self Care Products, Cosmetics, Biocides, Food Supplements, with proven experience in every developmental stage of drug lifecycle and the latest innovations.
Exceptional competence in corporate quality control and effective stakeholder negotiator for CROs, Clinical Laboratories, Biotech requirements and Private Funding, as well as On-site Audits including facilities. Excellent leadership and communication skills with experience as an Associate Director of a CRO managing a department of five staff, maintaining optimum levels of performance and productivity.
