Please contact us for a free consultation on your projects.

In order to set a teleconference with our clinical research team and/or submission of request for proposal, please contact ;

Julie Locke, Director of Business Development
Phone: 905-918-2727
E-mail: j.locke@krgi.org

Kriger Research Group International provides clinical research services for pharmaceutical and biotechnology product development from phase II through phase IV for US, Canadian, European and multinational pharmaceutical companies. KRGI is your way to high quality design, conduct and analysis of clinical trials.

Our staff, zealously live and breathe their projects, providing meticulous attention to the details. They ensure that executions are crisp, timely, and accurate. You receive truly personal service - and our senior management gives you their attention.

CLINICAL TRIAL MONITORING

Clinical Monitoring

KRGI commits to provide sponsor with highly qualified regional based Clinical Research Associates which substantially reduces the overall cost of the project and ensures its timely completion. We have experienced staff in most geographical regions. This sets KRGI apart from other CRO-s that might not have such extended capabilities.

• KRGI CRA-s perform comprehensive site management and monitoring activities to include the following types of monitoring visits:
  • Pre study qualification visits
  • Initiation visits
  • Interim monitoring visits
  • Close out visits

All activities are performed in accordance with ICH-GCP to ensure all investigational sites are compliant with all applicable regulations and protocol requirements.

• The paramount responsibility of KRGI CRA-s is to ensure timely subjects recruitment, patient rights, safety and data integrity.

In addition to on-site responsibilities each CRA is responsible for site management documentation and follow-up activities to ensure that site staff remains motivated and focused.

In summary the KRGI CRA plays a major role in the successful conduct of a study. The relationship developed between the CRA and the site staff is such that there is a focus on open effective communication with the CRA providing training and support thus ensuring patient safety, data quality and maximizing patient enrolment.

Medical Monitoring:

• Medical Monitoring (including 24/7 Medical Monitor coverage)
• Enhancement of regulatory compliance.
• Clarifying inclusion/exclusion criteria with the investigator.
• Providing consultation for potential safety issues or medical concerns regarding the clinical study.

 

 

REGULATORY AFFAIRS

Clinical trial registration/licensing

Our experience encompasses obtaining clinical trial approvals and registration of new chemical, biological entities and medical devices. We can also provide assistance with post-registration activities, such as variations and renewals.

Regulatory submissions

Our regulatory team includes professionals with over 20 years of experience in dealings with FDA.(USA), TPD (Canada) , EMEA (European Union).TGA (Australia and NZ) and similar agencies in other countries

Safety reporting

Patient safety and regulatory compliance are our primary concerns when conducting clinical studies. We work closely with our client's own drug safety department to provide safety surveillance and prompt, accurate reporting of serious adverse events.

 

 

CLINICAL TRIAL MANAGEMENT

Project management

Our project management team works closely with the scientific team to ensure the smooth progression of your clinical trial. Our Project Managers work effectively and diligently to manage all critical aspects of the study to ensure on-time delivery of results, within budget and with the highest possible quality output. Our team will work with you on all aspects of the trial from the first regulatory submissions through to closeout and final reporting to help you and your project succeed.

We provide:

• Frequent and timely reports to our sponsors.
• Training for CRA-s and site personnel on the protocol, CRF-s, SOP’s, ICH- GCP.
• Constant review of CRA-s work to assure highest standards and consistency
• Management of Budget and Project Timelines

 

 

QUALITY ASSURANCE

Investigative sites audit

• We verify that the protocol is performed according to Good Clinical Practices (GCP) and International Commission on Harmonization (ICH) standards and the sponsor's or CRO-'s Standard Operating Procedures (SOPs).
• Review the informed consent content and process
• Review records and procedures concerning interactions with the IRB.
• Review records and procedures concerning drug accountability
• Inspect study-required facilities and equipment
• We verify that the data collected in a representative sample of Case Report Forms (CRF-s) are supported by source documents.
• Assess compliance with internal SOPs
• Study documentation audit
• Verify that the protocol is performed according to GCP and ICH standards.
• Review records and procedures for site visits
• Review study file documentation
• Ensure internal systems used in the conduct of clinical trials are correct, including SOPs for Adverse Experience (AE) reporting, supplies distribution, and data handling.
• Assess compliance with internal SOPs
• Compare study report versus the protocol, CRF-s, and database.
• Ensure internal consistency in reports
• Preparation for regulatory inspection

Covering:

• Trial master file audits
• System audits
• Site audits
• Central laboratory audits
• Data base audits
• Final clinical report audits

 

 

 

DATA MANAGEMENT

Our clinical data management team is using the most advanced and comprehensive clinical data management software available and according to the highest regulatory standards to ensure auditable GCP quality results, and with the required levels of efficiency to keep your drug development and medical device programs on track.

Our data management services include:

• Web-based e-trials
• Electronic Data Capture in full compliance with 21CFR part 11
• Case Report Form annotation and Data Handling Manual
• Blind and independent double data entry
• On-demand comprehensive data validation reports
• Full electronic Audit Trail
• Computer-generated and fully tracked Data Clarification Forms (queries).
• Autoencoders for MedDRA, WHO adverse events and medications, COSTART, or your custom dictionary
• Database export to custom ASCII or SAS-AE with code list libraries and variable labels
• CRF scanning
• Archival to CD-ROM
• Reconciliation of safety database vs. study database

KRGI specializes both in new drugs and medical devices clinical trials

• Anesthesiology
• Cardiovascular
• Dental/Maxillofacial Surgery
• Dermatology/ Plastic Surgery
• Dialysis
• Endocrinology
• Gastroenterology
• Hematology
• Immunology/ Infectious Diseases
• Musculoskeletal
• Nephrology/Urology
• Neurology
• Obstetrics/Gynecology
• Oncology
• Ophthalmology
• Otolaryngology
• Pain Management
• Pharmacology/Toxicology
• Pediatrics/Neonatology
• Psychiatry/Psychology
• Pulmonary/Respiratory Diseases
• Respiratory
• Rheumatology
• Spinal Cord Trauma
• Transplantology
• Trauma/Emergency Medicine
• and some other areas

Kriger Research Group International is a leader in providing professional development programs for clinical research professionals. These programs are designed to provide a focused course of study for individuals seeking to position themselves in the clinical research and pharmaceutical trials industry as a clinical research associate, clinical research coordinator and data management specialists. They also provide knowledge and skills of clinical excellence in monitoring scientific studies toward the advancement of knowledge and improvement of health. Regarding training please review: http://www.krigerinternational.com

Headquarters (Toronto) Bruce Kriger, Director Huntsville, Ontario Canada P1H 1K6 Phone: 905-918-2727 Fax: 705-635-9292 E-mail: bruce@kriger.ca	Andover, Massachusetts 300 Brickstone Square Suite 201 Andover, Massachusetts 01810 United States Phone/ Fax: 1-508-342-7006 E-Mail: andover@krgi.org
Baltimore, Maryland 400 East Pratt Street 8th Floor Baltimore, Maryland 21202 United States Phone/ Fax: 1-410-558-6458 E-Mail: baltimore@krig.org	Chicago, Illinois 70 West Madison St. Three First National Plaza Suite 1400 Chicago, Illinois 60602-4270 United States Phone/ Fax : 1-312-276-8777 E-Mail: chicago@krgi.org
Jersey City, New Jersey One Exchange Place Suite 1000 Jersey City, New Jersey 07302 United States Phone/Fax: 1-201-604-6116 E-Mail: jerseycity@krgi.org	New York City, New York 845 Third Avenue New York City, New York 10022 United States Phone/ Fax :1-212-937-2459 E-mail: newyork@krgi.org
Philadelphia, Pennsylvania 1500 Market Street 12th Floor, East Tower Philadelphia, Pennsylvania 19102 United States Phone/Fax: 1-215-352-0855 E-Mail: philadelphia@krgi.org	San Antonio, Texas 1777 NE Loop 410 Suite 600 San Antonio, Texas 78217 United States Phone/Fax : 1-210-568-6933 E-Mail: texas@krgi.org Web: http://www.kriger.com
San Francisco, California 71 Stevenson Street Suite 400 San Francisco, California 94105 United States Phone/Fax: 1-415-651-9288 E-Mail: sanfrancisco@krgi.org	Seattle, Washington Seafirst Fifth Avenue Plaza 800 Fifth Avenue Suite 4100 Seattle, Washington 98104 United States Phone/ Fax: 1-206-260-1333 E-Mail: seattle@krgi.org
Tampa, Florida 2202 N. West Shore Blvd Suite 200 Tampa, Florida 33607 United States Phone/Fax: 1-813-315-7118 E-Mail : tampa@krgi.org	Montreal , Quebec 1000 de La Gauchetiere Street West 24th Floor Montreal, Quebec, Canada H3B 4W5 Phone/ Fax: 1-514-221-2156 E-Mail: montreal@krgi.org
Vancouver , BC 885 West Georgia Street Suite 1500 Vancouver, BC, Canada V6C 3E8 Phone/ Fax: 1-604-357-1144 E-Mail: vancouver@krgi.org	Tel-Aviv, Israel 108 Levinsky St. #5336 Tel Aviv, Israel 61592 Toll Free: 1-800-282-811 Tel:+972-3-688-7061 Fax: +972-3-7617083 E-Mail: krc_israel@kriger.com
Bejiing, China Dr. Henry Sun, President Dr. RongHong Zhu, Vice President for Operations Dr. Jason Guo, Vice President for Science Dr. Ying Wang, Assistant to the Presidents Beijing ClaiO Science and Technology Co., Ltd. Suite A111, 6th floor Jin Yuan Center, #1 Yuanda Road, Haidian District, Beijing, China. Tel: 022-26736062, 022-26736580 Fax: 022-26736587 E-mail: j.locke@krgi.org	Hyderabad, India 301 KHR building, Humayun Nagar Hyderabad.INDIA. Phone: +91-40-66365636 Cell : +91-9985706290 E-mail: j.locke@krgi.org London, UK 90 Long Acre Covent Garden London, WC2E 9RZ UK Tel: +44 (0) 203 002 7945 E-mail: j.locke@krgi.org

Please contact us for a free consultation on your projects.

In order to set a teleconference with our clinical research team and/or submission of request for proposal, please contact ;

Julie Locke, Director of Business Development
Phone: 905-918-2727
E-mail: j.locke@krgi.org

Contact Information

Kriger Research Group International
Tel-Aviv, Israel Office
108 Levinsky St. #5336
Tel Aviv 61592 Israel
Phone: +972-3-688-7061
Fax: +972-3-7617083
E-mail:

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