GMPintro

GMPintro is the premier choice for healthcare manufacturing facilities seeking to achieve global GMP certification and regulatory compliance.
Our comprehensive service portfolio includes consultancy, training, and advanced turnkey solutions tailored to meet the stringent requirements of WHO, FDA, EMA, and other regulatory authorities worldwide.
We provide the services following:
a) All applicable laws and regulations including; without limitation, the FDA, EMA, EDA, GCC, WHO, and specifically including standards of GMP, GLP, and GEP; and
b) The standards and practices are generally accepted in the industry and exercised by others performing similar services.

What sets GMPintro apart is our unwavering commitment to excellence and cutting-edge solutions in medical manufacturing compliance.
We offer more than just consultancy—we provide a transformative partnership focused on enhancing operational efficiencies and ensuring regulatory adherence.
Our deep industry expertise, , empowers us to deliver tailored solutions that exceed expectations and drive tangible results.
Whether navigating intricate regulatory landscapes or streamlining operations , we are dedicated to empowering our clients to thrive in a rapidly evolving global market..

Founded on a legacy of expertise and integrity, GMPintro comprises a team of industry pioneers and former regulatory experts. With over 20 years of combined experience in the pharmaceutical & biotech sectors, and a proven track record of success across diverse regulatory environments (including Egypt, Emirates, Jordan, Saudi Arabia, India & Iraq), we bring a wealth of experience to every client partnership.