About Scope international ag
SCOPE International AG: Your Trusted Partner in Clinical Development and Consulting Services
SCOPE International AG is a leading full-service Contract Research Organization (CRO) that provides clinical development and consulting services to the pharmaceutical, biotechnology, and medical device industries. With a network of 16 local offices and business entities throughout Europe and the USA, SCOPE offers its clients comprehensive support for their clinical trials.
At SCOPE International AG, we understand that every client has unique needs when it comes to clinical development. That's why we offer customized solutions tailored to meet each client's specific requirements. Our team of experts has extensive experience in all phases of clinical research, from early-phase studies to post-marketing surveillance.
Our Services
SCOPE International AG offers a complete range of services designed to support our clients' clinical development programs. These include:
1. Clinical Trial Management: We provide end-to-end management of your clinical trials, including protocol design, site selection, patient recruitment, monitoring, data management, statistical analysis and reporting.
2. Medical Writing: Our experienced medical writers can help you prepare high-quality documents such as protocols, Investigator Brochures (IBs), Clinical Study Reports (CSRs), regulatory submissions and scientific publications.
3. Regulatory Affairs: We provide regulatory affairs support for all stages of drug development from preclinical through post-marketing activities including preparation of IND/CTA/NDA/MAA submissions as well as interactions with regulatory authorities worldwide.
4. Pharmacovigilance: Our pharmacovigilance team provides comprehensive safety monitoring services throughout the lifecycle of your product including signal detection & evaluation; risk management planning; safety database setup & maintenance; case processing & reporting; literature surveillance & review; aggregate report writing & submission.
5. Quality Assurance: We offer quality assurance services such as auditing (GCP/GLP/GMP), SOP writing/reviewing/updating/training etc., vendor qualification/management, and CAPA management.
Our Approach
At SCOPE International AG, we believe in building strong relationships with our clients. We work closely with you to understand your needs and develop customized solutions that meet your specific requirements. Our team of experts has extensive experience in all phases of clinical research, from early-phase studies to post-marketing surveillance.
We are committed to providing high-quality services that meet or exceed our clients' expectations. Our team is dedicated to ensuring that every project is completed on time, within budget, and with the highest level of quality.
Why Choose SCOPE International AG?
1. Experience: With over 20 years of experience in the industry, SCOPE International AG has a proven track record of success in clinical development and consulting services.
2. Expertise: Our team of experts has extensive experience in all phases of clinical research, from early-phase studies to post-marketing surveillance.
3. Quality: We are committed to providing high-quality services that meet or exceed our clients' expectations.
4. Customized Solutions: We offer customized solutions tailored to meet each client's specific requirements.
5. Global Presence: With a network of 16 local offices and business entities throughout Europe and the USA, we can provide support for your clinical trials wherever you need it.
Conclusion
SCOPE International AG is an independent full-service CRO that provides comprehensive support for clinical development programs across the pharmaceuticals, biotechnology and medical device industries worldwide. With over 20 years’ experience in this field coupled with a global presence through its networked offices across Europe & USA; SCOPE offers customized solutions tailored specifically towards meeting each client’s unique requirements while maintaining high standards for quality assurance throughout every stage from protocol design through regulatory submissions up until post-marketing activities such as pharmacovigilance monitoring etc., making us your trusted partner for all things related to Clinical Development & Consulting Services!
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