Your CRO of choice for WOMEN’S HEALTH

WOMEN’S HEALTH

SCOPE International is an international contract research organization (CRO) with a proven track record in successfully delivering phase I through phase IV studies in all major indications, including pediatric trials, orphan drugs, biologics, and medical devices, non-interventional studies (NIS), and post-authorization studies. Using our close connections with leading investigators and key opinion leaders, we believe in providing the highest quality solutions worldwide.

For the last 20 years, SCOPE has been at the forefront of delivering trials in Women’s Health, focusing on the many unmet medical needs and working to improve existing drug and device therapies in both reproductive health, age-related conditions, and other indications.

SCOPE has the distinct ability to consistently provide expertise to deliver the recruitment and treatment goals for Women’s Health clinical trials on time and on budget. In business since 2000, we have conducted more than 260 studies with over 70,000 patients worldwide. We have offices in 14 countries across Europe and Ukraine operating with 250 permanent employees covering more than 30 countries and all major markets.

EXPERIENCE IN WOMEN’S HEALTH

  • ART, e.g. IVF, ICSI

  • Endometriosis

  • Contraception

  • Postmenopausal Complaints

  • Vulvar and Vaginal Atrophy

  • Vaginitis

  • Rheumatoid Arthritis

  • Fibromyalgia Syndrome (FMS)

  • Polymyalgia Rheumatica

  • Oncology

  • Pain Management

  • Obstetrics

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WOMEN ́S HEALTH STUDIES
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SITES
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SUBJECTS

OUR SPECIALIST

Dr. Michael Binder, Director Operations at SCOPE International

Dr. Michael Binder
Women’s Health Expert

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STUDY DESIGN AND MANAGEMENT

By utilizing more than two decades of industry experience, coupled with the professional experience of our staff, SCOPE provides a well-established approach for successful Women’s Health trials.

HERE’S WHAT SETS US APART:

 

  • Highly experienced project team
  • Specific clinical Women’s Health study expertise gathered over more than 20 years of experience
  • Strong global network of investigators in Women ́s Health
  • Expertise in implementing advanced technology solutions improving study outcomes
  • Anticipation and contingency planning to avoid pitfalls which only experience can predict

ACCURATE AND APPROPRIATE FEASIBILITY

Recruitment is pivotal in achieving the desired outcome of a study. The SCOPE team is highly experienced in developing therapeutically appropriate and insightful feasibility questionnaires and extrapolating this to our enrollment plans. Our teams recognize that feminine healthcare has considerable variability in different settings across countries and local cultures, thereby requiring sensitivity and local knowledge. SCOPE therefore conducts a feasibility survey to confirm projected recruitment rates and utilizes feedback from local Principal Investigators (PI) as part of our standard proposal process.

SITE TRAINING AND QUALIFICATION

SCOPE project teams are experts in the design and delivery of site training to ensure protocol-consistent enrollment and efficacy assessments, using electronic data capture systems (EDC, eCOA e.g. ePRO) and innovative study tools including our own project management tool.