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ASKA Research develops and markets quality custom products and tools to assist you in your clinical research program activities. All of our products meet or exceed recognized industry standards. For details on all of our products or to order, call (604) 736-3166 or e-mail us at products@askaresearch.com.

RAN Products and Online Training
ASKA Research is the official Canadian provider of reference manuals and products by Dr. Ruth Ann Nylen of The RAN Institute. Publishers of the Ultimate Step-by-Step Guide for Conducting Pharmaceutical Clinical Trials in the USA, the RAN Institute provides reference manuals, GCP flash cards and high-quality online GCP training for Sponsors and Monitors as well as Investigators and Clinical Research Coordinators. ASKA and the RAN Institute is excited to announce the recent development of a RAN Institute Ultimate Step-by-Step Guide that includes Canadian content. Please contact ASKA Research directly for details of pre-launch pricing or to register your interest.

These guides are useful for:
  • training new personnel
  • reference for experienced professionals
  • study and review for Certification Exams

Comprehensive guides contain:
  • overviews of clinical trials including descriptions of relevant regulations and where to find the most current regulations
  • details of the more than 50 steps necessary to complete before, during, and after a clinical trial
  • detailed regulation and guidelines references that support the requirements for each step
  • sample forms, documents, checklists and letters that ensure compliances with regulations
  • practical hints and tips

For more details, visit the ASKA Research Training Campus

Standard Operating Procedures (SOPs)
ASKA Research develops and customizes Standard Operating Procedures (SOP) for your company or investigative site.

The ASKA Research's clinical SOPs for monitoring and managing clinical trials provide comprehensive guidelines in accordance with ICH/GCP. These SOPs include direction on safety reporting and pre-study qualification, site initiation, monitoring, study closure visits and associated trial activities.

The ASKA Research Investigative Site SOPs provide comprehensive site study management guidelines in accordance with ICH/GCP.

ASKA Research SOPs support Quality Assurance Compliance measures by providing detailed written guidelines to achieve performance uniformity for a specific function, particularly the implementation of FDA, Health Canada & ICH/GCP Guidelines.

 
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