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Clinical Development Planning
ASKA Research's Clinical Development services include assessment, analysis and preparation of risk-benefit evaluations that assist you in developing business strategies.
Regulatory Services
Our Regulatory Services encompass the preparation and submission of dossiers to obtain country-specific approvals to conduct clinical trials.
Project Management
ASKA Research's Project Management includes directing and controlling all critical facets of your study such as site selection and ICF and CRF design. In addition to expertise in current standards of research practice, time and budget management, ASKA Research's project managers offer excellent leadership, training evaluation and communications skills.
Lead Clinical Research Associate
ASKA Research's highly trained Lead CRAs provide the proven leadership skills required to coordinate and direct monitoring teams.
Monitoring/Clinical Research Associates (CRAs)
The ASKA Research Professionals Network (RPN) is a nation-wide, regionally based network of CRAs available for monitoring in any region in Canada. Monitoring services are also accessible through our collaborative partner organizations and our CRO alliance partners in the United States, Australia, Europe and the Asia-Pacific region. Our monitoring services encompass all quality control aspects of single or multi-centre clinical research trials.
ICH/GCP and Customized Training
ASKA Research delivers custom designed seminars to meet your training objectives. Our custom seminars are based on learner needs assessments and we award ASKA Research training certificates upon successful completion. Our lead trainer is company president Valerie Willetts, an ACRP Credentialed Clinical Research Trainer (CCRT) and the only Canadian with this designation. Depending on the training needs, we draw upon a pool of experts who regularly train on the behalf of ASKA Research.
Quality Assurance (QA)
Our Quality Assurance (QA) measures ensure that your clinical development plan is performed in compliance with ICH/GCP and applicable regulatory requirements and that data is generated, documented and reported accordingly. Our ASKA Research Professionals Network (RPN) includes experienced monitors and auditors at your disposal.
Clinical Research Meeting Planning
Meeting planning involves the development of meeting plans, budgets and the coordination and facilitation of all aspects of Clinical Research meetings. The project's objectives and critical program elements are identified and maintained as the central focus.
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