MEET PARTNERS IN CLINICAL RESEARCH
Founded in 1994
Accuracy and flexibility are defining aspects in the life of Partners in Clinical Research.
We have been involved in clinical research in North America since 1994.
Our expertise encompasses a wide variety of research studies and clinical trials in Phases I-IV.
We are well versed in electronic eCRFs and have worked in many different systems including Medidata-Rave, iMedNet, Medrio, InForm, DocuPhase, CTMS, eCaseLink, BioClinica and other sponsor proprietary systems.
We conduct on-site and remote field monitoring visits including
evaluations, initiations, ongoing study monitoring and closeout visits.
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We assist in preparation for FDA, Health Canada and sponsor audits.
INDICATIONS
We have extensive experience in the following therapeutic areas.
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CARDIOVASCULAR
CNS
ONCOLOGY
ONCOLOGY
Congestive Heart Failure, Hypertension, Atrial Fibrillation, Atherosclerosis, Angina, IIb/IIIa Inhibitors, Deep Vein Thrombosis, Acute Cardiac Syndrome
Alzheimer, Partial Seizures, Chronic Pain, Schizophrenia, Stroke
Metastatic Breast, Pancreatic, Myelogenous Leukemia, Glioblastoma, NSCLC,
Cholangiocarcinoma,
Advanced Solid Tumor Lymphoma
IMMUNOLOGY
INFECTIOUS DISEASES
PAIN MANAGEMENT
Kidney, Liver and Heart Transplant, Rheumatoid Arthritis.
Oral Candidiasis and HIV
Cancer Related,
Chronic Non-Cancer Pain,
Diabetic Neuropathy,
Persistent Back Pain
PULMONOLOGY
MEDICAL DEVICES
OPTHAMOLOGY
Asthma, Pulmonary Hypertension, Chronic Acute Bronchitis, and Geriatric Pneumonia, COPD, Pulmonary Hypertension
Stent Delivery System,
Ocular Steroidal Delivery System
Diabetic Retinopathy,
Macular Degeneration, Uveitis,
Herders Disease (LHON)
ENDOCRINOLOGY
UROLOGY
Diabetes Type 1 and Type 2,
Diabetic Nephrology, Inhaled Insulin
Nocturia
OVERVIEW OF COURSES OFFERED
Flexible Enrollment
INTRODUCTORY COURSE
This course provides an introduction to clinical trial research for the drug or device development process. Provides history, methodology, rationale, regulations, and Good Clinical Practices (GCP).
On-Site or Web-Based
RESEARCH SITE PREPARATION
This class will help you and your staff set-up the ideal research site that meets sponsors' needs. Everything from negotiating site contracts, setting up files and source documents, regulatory requirements, collecting data, informed consent procedures, drug management overview, file management, patient recruitment and preparing for monitoring visits and audits.
Web-Based
CRA TRAINING
This class will prepare you will all the necessary skills to be a Clinical Research Associate. This class includes introduction to clinical research, GCP training, communication and interpersonal skills, methods and procedures, step-by-step instructions for conducting evaluation, routine monitoring visits, close-out visits. Tips on managing multiple studies and multiple sponsors if needed. Regulations for Canada and the USA.