Services
Whether your project requires a specific area of support or a total drug development solution, ASSOCIATED MEDICAL GROUP offers a comprehensive suite of clinical services to meet your needs. Delivered by people who understand your world.
SERVICES IN PHASE I - IV
Dose ranging, safety and tolerability
Proof of Concept
Pilot studies on new dosage forms and delivery systems
PPK/PD studies
Special populations children, renal and kidney impaired populations, patients suffering cancer, CNS etc.
Renal and kidney impaired populations
Compassionate use trials
ADME trials
Genotyping
Full Service and Consulting for Bioequivalence
Feasibility Studies
Development planning and strategy
Selection and training of investigators
Eligibility validation
Grant and contract negotiation
Preparation of investigators' meetings
Administration of investigators' grants
Administrative controls to complete project on schedule and within budget
Remote data entry systems
Secure web based data entry
Detailed status reporting
Source documentation auditing
Adherence to GCP
Drug accountability
Data review and correction
AE and SAE reporting
24 h/ 7 day capability to handle situations which require immediate attention
Detailed in-house monitoring
Dose ranging, safety and tolerability
Proof of Concept
Pilot studies on new dosage forms and delivery systems
PPK/PD studies
Special populations children, renal and kidney impaired populations, patients suffering cancer, CNS etc.
Renal and kidney impaired populations
Compassionate use trials
ADME trials
Genotyping
Full Service and Consulting for Bioequivalence
Feasibility Studies
Development planning and strategy
Selection and training of investigators
Eligibility validation
Grant and contract negotiation
Preparation of investigators' meetings
Administration of investigators' grants
Administrative controls to complete project on schedule and within budget
Remote data entry systems
Secure web based data entry
Detailed status reporting
Source documentation auditing
Adherence to GCP
Drug accountability
Data review and correction
AE and SAE reporting
24 h/ 7 day capability to handle situations which require immediate attention
Detailed in-house monitoring
MEDICAL WRITING
Protocol development and writing
Investigators brochure development and writing
CRF and eCRF development (also printing and distribution)
Monitoring manuals
Translation services in all local CEE languages
Medical marketing scripts
Graphic displays & slides for scientific or Corporate meetings
Protocol development and writing
Investigators brochure development and writing
CRF and eCRF development (also printing and distribution)
Monitoring manuals
Translation services in all local CEE languages
Medical marketing scripts
Graphic displays & slides for scientific or Corporate meetings
VETERINARY CLINICAL TRIALS:
Studies:
Dose finding studies
Dose confirmation studies
Field efficacy&safety studies
Field efficacy compared to competitors
Services:
Site selection including laboratories
Set up of studies
Training of study participants
Monitoring of studies including regular site visits
Data collection and cleaning
Prepare master study file
Drug accountability
Data review and correction
Administrative controls to complete project on schedule and within budget
Source documentation monitoring
Development planning and strategy
Studies:
Dose finding studies
Dose confirmation studies
Field efficacy&safety studies
Field efficacy compared to competitors
Services:
Site selection including laboratories
Set up of studies
Training of study participants
Monitoring of studies including regular site visits
Data collection and cleaning
Prepare master study file
Drug accountability
Data review and correction
Administrative controls to complete project on schedule and within budget
Source documentation monitoring
Development planning and strategy
