Max Neeman International Headquartered in New Delhi, India, Max Neeman
International is an ISO certified Contract Research Organization with the expertise
to assist pharmaceutical, biotech and device industry in all aspects of conducting
clinical trials in India and worldwide.
As the clinical research division of healthcare consortium ‘Max India’, Max Neeman
International has the backing of this $1 billion life sciences consortium, owning
twelve hospitals and managing other healthcare businesses in life insurance,
healthcare and clinical research.
Highlights
Full service CRO with focus on Phase I to IV clinical trials for drugs, pilot and pivotal medical device studies
90% of employees are Physicians (MDs) and ICH GCP trained (Clinical Research Coordinators/Project Managers/ Clinical Research Associates)
Offices strategically placed across cities throughout India, increasing recruitment, sustaining hospital relationships, and attracting top talent
175 active sites in 22 cities, maintained relationships with 800 ICH GCP trained Investigators and a patient pool of 8–10 million
Data from multiple global trials included for U.S. NDA approval from pivotal Phase III studies
Ongoing clinical services to 8 of the top 10 global pharmaceuticals plus biotechnology firms
Certification: ISO 9001:2008 certified by United Kingdom Accreditation Service (UKAS) for Site Management, Monitoring and Data Management
Certification: ISO 27001 certification for ISMS (Information Security Management System) under process
Partnerships with USA and Europe based clinical research organizations for global trials
Partnerships with numerous CAP accredited central labs throughout India
Max Neeman Milestones:
Established Practice and Site Management services began in 2001
First U.S. FDA GCP audit occurred and Monitoring services were initiated in 2005
Data Management Centre was set up and operations began in 2006
170th trial awarded in 2009, across 8 of 10 top U.S. Pharmas and numerous Biotechs; 50th clinical trial awarded in 2007 and ISO 9001:2000 certifi cation achieved
Four successful FDA audits, combined with forty sponsor, regulatory body audits and multiple site audits, to date