Clinical and Regulatory Services

TrialMed Life Sciences, LLC
www.trialmed.com ; email: raj@trialmed.com ; Ph: 714-658-3039

Provides pin point regulatory strategies to start-up companies to make sure the company’s goals and objectives are achieved in timely manner.
Ensuring the clinical trial is conducted according to FDA GCP guidelines. TrialMed's monitoring and auditing is conducted per FDA guidelines in the United States and countries like Taiwan, Brazil, India and Singapore. This allows companies save time and burn rate and increase the valuation of their medical technology.
Use "PatientFast" recruitment strategies and a network of top notch physicians investigators and clinical monitors in the U.S, Taiwan, Brazil,India, and Singapore to enroll fast and make a clinical trial one of the best studies.
Experience in maintaining patient’s safety and privacy in accordance with the
HIPAA regulations and PHI statutory law.
Provide patient recruitment strategies for
quick enrollment and develop clinical marketing strategies for post PMA status.
Dialog with FDA and international regulatory authorities to evaluate the
safety and efficacy of the medical product to meet the clinical need
www.TrialMed.com
USA, INDIA, TAIWAN, SINGAPORE, TURKEY, MEXICO & BRAZIL

TrialMed Life Sciences, LLC
Location: Irvine, Ca
International Office: Mumbai, India

Contact: Dr Raj Nihalani, MD, RAC(US)
Cell: 714-658-3039
Email: raj@trialmed.com or accessclinicaltrials@yahoo.com
www.trialmed.com