Medical Scientific Consulting
Pre-Clinical | Phase I to III | Market Access | Phase IV | Drug Marketing
As a part of our standard operating procedures, CCR provides important details for each step of the clinical study to the Project Managers to meet the unique meets of our clients.
CCR provides:
CCR project manager ascertain every facet of the study requirements
Planning and coordination of the clinical development program
Meeting the requirements of a (future) benefit dossier
Preparation of all medical and epidemiological modules of a user dossier
Medical Pharmacovigilance / Safety
Development and implementation of a comprehensive and customized safety plans are essential to research.
CCR provides:
Review of medically coded data on adverse events and concomitant medications data
Vigilant monitoring for Adverse Events
Vigilant monitoring for Adverse Events
Investigator team training on safety reporting and clarification of safety related queries during Interim Monitoing Visits
Maintaining updated safety database for clinical trials
Support SAE reconciliation between clinical and safety database
Medical Affairs
CCR has been involved for many years in several phase II-IV, post marketing, registries and observational studies with large number of patients.
CCR provides:
Enhance the full exchange of scientific information
Ensure safe and proper adoption of a production
Commercialization
Meeting support
Medical Review
Delivering high quality, evidence-based, independent specialty matched medical review services that are cost effective, expedient and objective.
CCR provides:
Investigator Brochure
Protocol
CRF
Informed Consent
Study Manual
Statistical Analyses Plan
Data validation Plan
Study Reports
SAE narratives
Medical Writing
Providing special skills to produce well-structured documents that present information clearly and concisely.
CCR provides:
Clinical Trial Protocols
Case Report Forms
Clinical Trial Reports
Patient information leaflets
Patient information
Marketing Brochures
Regulatory Documents
Educational medical writing
Consulation
Training Services
Study design
Investigator Brochures
Clinical Development Plans
- complying with regulatory, journal, or other guidelines in terms of content, format and structure.
Medical Marketing
Grow your profits, build your reputation and attract patients and cases you want.
CCR provides:
Website Development
Strategic Plan Development
Social Media Strategy
Retreat PLanning
Referral Physician Relations
Patient Service Enhancements
Newsletter
Direct Mail
Marketing Plans
Creative Ad Campaigns
Brochures and Patient
Education Material
Branding
Publication Writing
Our medical writers create documents that effectively and clearly describe research results, product use and other medical information.
CCR provides:
Competitive analyses
Original Research
Review Article
Clinical case study
Clinical Trials
Perspective, opinion and commentary
Study summaries
Book reviews
Literatur Search
Regulatory Affairs
We are working with experts in ethics and regulatory submissions for all European countries and some other countries worldwide.
CCR provides:
An ethics and regulatory expert team will work with the local ethics committees and regulatory offices
Providing the investigators with ethics and regulatory approvals in their countries
Expertise in international rules and regulations
Results within a short period of time
Are you interested in our services?
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