An understanding of country Health Authority regulations and requirements, combined with access to trained Investigators and Research professionals who have access to patient populations across various therapeutic areas, enables our consultants to support Sponsors to successfully initiate, manage and deliver clinical trials in the region.

Delivery of Clinical Operation and Trial management services, meeting Pharmaceutical Industry Standards . Innomas partners with Investigators and Research Professionals to provide rigorous, comprehensive training from active Global Clinical Research professionals: Drug Research & Development Overview; ICH/GCP; Health Authorities, IRBs, Ethics Committees; Clinical Study Design; Clinical Trial Development; Clinical Trial Management; Investigator responsibilities; Site Training; ....an

Our experienced data management team provide solutions for Pharmaceutical and Biotech companies, from data entry to data cleaning from study start-up to database lock, delivering quality data on time. Benefit from our team location in the GMT timezone and data mangers with clinical backgrounds.

Let our experts help you set up your PV system operational and support services: EU QPPV, local affiliates, QMS, Audits, PV training and Compliance are just a few. Clinical trial drug safety management: Full GCP, GVP, GMP and GDP support immediately available to you. VPS PV experts are ISO 9001:2015, ISO 14001 and ISO 18001 certified.