Welcome to BioPlan Ltd.!

BioPlan for over 15 years provides complete & wide-ranging Regulatory Affairs services, including: Pre-Clinical Development, Import of Pharmaceuticals, Manufacture and Allied Health Products. BioPlan's chief professional supervisor is MSc. Pharm Guy Wagner; with over 25 years of experience as well as his wide-range and uncontested knowledge in all aspects of the pharmaceutical and allied industries, BioPlan possesses a unique status in the industry. BioPlan has a professional, dedicated & well-trained staff completely devoted to our clientele.

Experience
Founded in 1996, BioPlan Ltd. has over 15 years of operating experience while its founder, CEO & chief professional supervisor, MSc. Pharm Guy Wagner, has spent more than 25 dedicated years learning the industry.
This proficiency and expertise, combined with a cutting-edge practical knowledge of the pharmaceutical and allied industries, has earned BioPlan Ltd. international prestige and an industry reputation for excellence and efficiency. We are privileged to count many top-industry groups among our loyal clientele and have uncontested success and satisfaction rates.

Full Life-Cycle Support
BioPlan Ltd. provides your product with active hands on full and professional regulatory support from early development through licensing and thereafter during manufacturing and/or import.
We find legal and innovated solutions to any problem or difficulty that may arise at any stage of the process.

 
 
 
 

Developing New Product?
With our extensive experience in all stages of the pharmaceutical and allied industries; BioPlan Ltd. is in a unique position to help and support you develop new products from the idea stages up until early human clinical studies.
We find legal and innovated solutions to any problem or difficulty that may arise at any stage of the process.

 
 
 
 

All the services that BioPlan Ltd. provide are supplied with total and complete discretion. All data and documentation is treated with the upmost confidentiality.