These services are highly needed with current regulations upgrades and tightened pharmaceutical controls enforced by Regulatory bodies across the globe.
QMS and compliance services will help clients adhere to the highest global quality standards in a cost effective manner, these services include but not limited to :upgrading pharmaceuticals facilities Good Manufacturing Practices (cGMP) to the European EMA, American FDA and Gulf Central Committee (GCC)  standards, which will help clients to expand Access to key markets and provide high quality products to patients in these regions. Planned updates and training workshops are in place to help clients as well as key connections with authorities to facilitate Submissions and follow up:
1.Product development services:
LavidaPharma will have its own state-of-the-art pharmaceutical Product Development Lab and small scale production area. The current know how with Dr Ghazzal and proven track of providing high quality products formulas will help kick off project as well as contracting pharmaceutical drug developers to build certain expertise .Our aim to provide complete ready to use generic product files that can be submitted for registration all over MENA, Gulf Countries and Europe Product development work at LavidaPharma  will be done in accordance with  FDA/EU Current Good Manufacturing Practice (cGMP) regulations for product development.
2.Qualification and validation services:
LavidaPharma will provide these services to customers to qualify their facilities and equipment used for pharmaceuticals manufacturing, storage and distribution which is now an enforced regulatory requirement for GMP renewals
3.Commercallization and marketing:
Lavida pharma will provide innovative marketing tools and help developing marketing plan ,link to key distributors in the region
4.Strategy and Market Access:
Lavida pharma will provide access solutions to key markets and bridge access solution that provide faster track and better pricing