“Tailored Solutions, Driven by Your Goals”
We promise to deliver the best solutions to you
A Full-Service Experience
01
Policy Review and Development
Analyze and refine existing policies or develop new ones to align with public health objectives.
02
Policy Research and Analysis
Conduct in-depth research to inform policy-making and strategic decisions.
03
Research and Data Analysis
Comprehensive epidemiological studies, health assessments, and evidence-based reporting.
04
Health Communication
Crafting impactful communication strategies for health advocacy and stakeholder engagement.
05
Public Health Consulting
Offering expert advisory services for healthcare programs, strategies, and initiatives.
06
Project Management
End-to-end planning and execution of public health initiatives.
Special Flagship Offering
SOCRA CCRP Certification Preparatory Program
Preparation for the Certified Clinical Research Professional (CCRP) certification by SOCRA (Society of Clinical Research Associates). Designed for clinical research coordinators, investigators, pharmacists, project managers and monitors.
Pre-Program
Eligibility Screening & SOCRA Registration
Mandatory eligibility screening (SOCRA Category 1/2/3 + GCP status) and official SOCRA registration and document filing, at least 6 weeks before the exam date. Approved candidates receive the CCRP Reference Manual.
Day 1
Examination Framework & High-Risk Domain Refresher
Research Study Start-Up domain (40% of exam): trial phases I–IV, GCP ICH E6(R3), 21 CFR 50 & 56, 45 CFR 46 (Common Rule), IRB/IEC/REB, IND/IDE determination, FDA 1572, 3454, 3455, TMF, SIV and Informed Consent.
Day 2
Domain Reinforcement & Examination Strategy
Research Study Implementation domain (50% of exam): ALCOA+, CRFs, Investigational Product accountability, 21 CFR 312 & 812, AE/SAE reporting, MedWatch 3500/3500A, CAPA, DSMB, FDA 482/483 audit prep, study closeout and clinicaltrials.gov.
Day 3
Full Mock Simulation
Timed simulation matching the real CCRP format, score breakdown by domain (Start-Up, Implementation, Closure) and weak-domain identification.
Day 4
International Expert Review & Certification Governance
Led by international expert Dr. Dipti Sawant: mock review and rationalisation, CBT Prometric vs. ProProctor mechanics, the 65/65 question block mechanic and retest rules.
Day 5
Examination Day
Prometric Test Centre, Kuala Lumpur. 130 MCQs (100 scored, 30 unscored), 4-hour window, immediate score report.
Eligibility Categories
Category 1
At least 2 years full-time experience (or 3,500 part-time hours) in clinical research within the past 5 years.
Category 2
Degree in Clinical Research + at least 1 year full-time experience (or 1,750 part-time hours) within the past 2 years.
Category 3
Certificate in Clinical Research (≥12 credits / 144 contact hours) + Science, Health or Pharmacy degree + at least 1 year full-time experience (1,750 hours) within the past 2 years.
All candidates must also have experience with Good Clinical Practice (GCP), research involving human participants, and research under an IRB/IEC/REB-approved protocol.
Documents for SOCRA Filing
- Updated CV / Resume
- Academic degree certificate & transcripts
- Clinical research certificate / transcripts (Category 3)
- Employment verification / service letter on official letterhead
- Official job description
- Valid GCP certificate
Ready to check your eligibility and submit your documents?
Start eligibility screening →