CRM evaluates feasibility studies/request that are forwarded by sponsors/CROs and disseminates them to a large pool of potential investigators.
CRM assists investigators who are interested to take-on the trial to complete and submit the feasibility study/request to the sponsor or CRO.
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Complimentary feasibility studies are available through CRM.
Consultation and management of clinical trial budget
CRM advices investigators and sponsors/CROs on the clinical trial budget. This service ensures that resources are sufficient in order to complete all obligations of the clinical trial.
CRM manages the trial budget with full transparency and schedule reports to investigators and the sponsor/CRO (CRM charges a fee of 15% above the value of the trial budget which will be utilised to finance its operations and training programmes to up skill investigators and support staff).
Review of Clinical Trial Agreement (CTA) & Non-Disclosure Agreement (NDA)
CRM assists investigators & sponsors/CROs by reviewing and advising on Clinical Trial Agreements (CTAs) & Non-Disclosure Agreements (NDAs).
CRM’s experienced legal team will provide assistance to review the CTA/NDA.
Development & placement of study coordinators
CRM recruits suitably qualified candidates and trains them to become capable Study Coordinators (SCs) who will then be placed at trial sites in order to assist investigators.
CRM currently has a pool of 130 trained SCs based in major clinical research centres nationwide.
Training related to Clinical Research
CRM organizes various subsidized training programs for investigators and support staff in order to improve their capabilities to undertake ISR.
Refresher courses on Good Clinical Practise (GCP) are also held for doctors and support staff.
Sites capability improvement & enhancement
CRM improves the capability of sites by assisting in both systems and infrastructure improvements.
Growing the pool of investigators and sites
CRM continuously attracts and develops potential new investigators and sites in both the public & private healthcare system.
One-stop centre for the industry
CRM assists industry players in resolving issues or delays faced with government agencies and regulators (eg. BLESS, MREC, MDA, NPRA, IRBs) that may delay the approval or initiation of trials.
Improving public and patient awareness
CRM engages with a variety of patient support groups and NGOs, undertakes advertising and promotional events, and seeks to generate positive media coverage to spread the word about clinical research, generate goodwill and to facilitate patient recruitment.
Promoting Malaysia as a hub for Industry Sponsored Research (ISR)
CRM participates in domestic and international events to engage sponsors and CROs as well as to promote Malaysia as a choice destination for ISR.
CLINICAL RESEARCH MALAYSIA
D-26-06, Menara Suezcap 1
KL Gateway, No. 2 Jalan Kerinchi
Gerbang Kerinchi Lestari
59200 Kuala Lumpur
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