Pharmaceutical Market in KSA & GCC

The Market in KSA &GCC is expected to register a significant of 9% in the next 10 years expecting to reach $US 35 Billion by 2027 from current $US 16 Billion in 2016 .

Call Us

About us

Saudi Arabia strategic plan

1

Increasing local pharmaceutical Manufacturers.

2

Offering financial assistance to local Pharma manufacturers.

3

Offering all support for biopharmaceutical localization.

4

Protecting local brands against branded generics.

WHY US

vision

Future Biopharma KSA strives to develop affordable biopharmaceutical care solutions and enable Saudi pharmaceutical companies to be players in the global pharmaceutical market.

Mission

Continuous develop and upgrade the Pharmaceutical industry into world-class standards that implements cGMP, GCP, and GLP standards.

Continuous advice and play a consultative role in the Saudi healthcare system by working closely with the SFDA and the Ministry of Health in Saudi Arabia.

Facilitate the transfer of related technology and know-how.

goals

Improving patients' lives, Access to affordable medicines ensuring the sustainability of healthcare Systems.

Being a leading company for Biosimilar and niche therapeutic product.

Being a production hub for Saudi Arabia & GCC, the Middle East and North Africa

First phase

Strategic collaboration for sourcing biopharmaceutical products with complete technology transfer.

Secondary packaging for all dosage forms including.

temperature-controlled goods such as Biosimilar, MAbs, Vaccines, Hormones and blood derivatives.

Second phase

Primary filling for all dosage forms, bulk products or APIs under cGMP guidelines . Dedicated lines for Biosimilar, MAbs, Vaccines, Hormones and blood derivatives.

Third phase

Future Biopharma KSA will provide end-to-end solutions for development, technology transfer and manufacture of Biosimilar DS to cater the need. Future Biopharma KSA will provide full turn-key technology transfer-based process adaptation to meet cGMP requirements. Include cell line development, upstream, downstream and Q.C to full cGMP production aiming for higher quality and cost efficiency.