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Contract Development & Manufacturing (CDMO)Sourced

Case Study: Recipharm unifies quality operations across 14 sites with Veeva

Recipharm Case StudySourced & dated by Case Study Desk
Key facts · TL;DR
Company
Recipharm
Industry
Contract Development & Manufacturing (CDMO)
Challenge
12 legacy systems and paper across 14 global sites
Headline result
60,000 hours of manual work saved per year with Veeva Quality Cloud

Key results

60,000 hrs
manual work saved per year
with cost savings on maintenance, governance, and licensing
14 to 3
review and approval steps
change-control process in Veeva QMS
14 sites
quality processes harmonized
replacing 12 legacy systems

The challenge

Before adopting Veeva, Recipharm relied on 12 different systems as well as paper-based processes to manage quality and manufacturing operations across 14 global sites. The fragmented landscape made it hard to standardize quality processes and collaborate consistently with customers.

The solution

Recipharm standardized on Veeva Quality Cloud, unifying quality management on a single platform across all 14 sites. As part of the move it overhauled its change-control process in Veeva QMS.

Unified Quality and using one Veeva platform has resulted in a better and more efficient collaboration with our customers.

LA
Laura Prada Alonso
Corporate eQMS Program Manager, Recipharm

The results, in context

Consolidating onto one platform reduced manual work by 60,000 hours per year while lowering maintenance, governance, and licensing costs. Recipharm cut its change-control review and approval steps from 14 to three and harmonized quality processes across its 14 sites.

Products used

Veeva Veeva Quality CloudVeeva Veeva QMS