Medical Director: Michael L. Twede, M.D., FACOG, has been involved in clinical research for over 20 years.

Company Director: Michael R. Braun, BS, compliments the business and research needs of the organization with over 25 years of Pre-Clinical, Biomedical and Human Subject research experience.

ACRP CCRC, BS, BA, RN, BSN, MA and MBA graduated staff provide the "Core Company" link to business structure and Sponsor trial success

We conduct studies in Phases I, II, III and IV studies and Pilot/Pivotal medical device studies
Our center specializes in the following therapeutic areas:

• OB/GYN (Hormone Replacement, Post-Menopausal Vasomotor Symptoms, Contraception, Menstrual Cycle-Control, Vaginitis, Infertility/Endometriosis, Sexual Dysfunction)
• Anti-Infectives (Pneumonia, Bronchitis, Sinusitis, other)
• Endocrinology (Weight Loss, including but not limited to Appetite Suppression, Type I and II Diabetes Melitis)
• Pulmonary (Allergy, Asthma, Pulmonary Hypertension)
• Rheumatology (Rheumatoid Arthritis, Osteoarthritis, Back Pain)
• Cardiovascular (Post-MI, Hypertension, Angina, CAD, Congestive Heart Failure, Arrythmia)
• Urology (BPH, Urinary Incontinence, Urinary Tract Infections, other)
• Oncology (Cervical Dysplasia/Cancer, including but not limited to GYN)
• Psychiatric (Depression, Insomnia, Anxiety)
• Dermatology
• Pain (Chronic Pain)
• Spine indications
• Surgical Device Trials

PRO® has and continues to work with all major Pharmaceutical companies, many Medical Device companies, and other drug/sponsor companies. We do not list all sponsor experiences so that PRO® can maintain their Confidentiality

We maintain repeat business with our sponsors by providing quality work, exceeding enrollment minimums, and by performing constant improvement processes to meet sponsor needs.

Clinical Research Support Services
We have staff of experienced Clinical Research Coordinators who take pride in collecting and documenting data in a highly detailed and concise manner. We provide our sponsors with timely and clean data, and meet protocol goals for patient recruitment. We concisely manage regulatory (FDA required) aspects and coordinate the day-to-day requirements of study subject needs.

PRO® turn-keys:

• Patient recruitment for target enrollment
• An established patient database by Indication that is continually growing
• Regulatory documents required by the sponsor
• Institutional Review Board submissions
• Required IRB review reports (quarterly or annual as required)
• Budget/financial arrangements
• Study correspondence between the sponsor and investigational site
• Storage of all study materials at our facility and off-site archive location
• Experienced and Certified Clinical Research Study Coordinators
• Quality assurance process and procedures
• Experienced and trial interested Investigators

PRO's Medical Director, Michael L. Twede, MD, has over 20 years clinical and clinical trial experience.

Our physician network totals more than 30 licensed and/or board-certified providers throughout Utah, Colorado and Nevada. Principal and Sub Investigator staff maintain CITI/NIH and other Human Subject Welfare and Safety training. They attend all Sponsor provided meetings and dedicated time to Study Monitors.

As principal investigators, our physicians are dedicated and motivated to provide the highest quality patient care. Our network and therapeutic area of expertise is ever increasing.

Our Organizational chart includes a Company Director, Medical Director, Phone Recruiter, Administrative, Budget/Financial/Regulatory and CRC/CCRC staff. PI and SubI staff affiliates work exclusively with PRO®

Industry specific Certifications are held by staff. GCP, ICH and Human Subject and Welfare training are held by all.

Cardiology/Vascular Diseases
Dermatology/Plastic Surgery
Endocrinology
Immunology/Infectious Diseases
Musculoskeletal
Nephrology/Urology
Obstetrics/Gynecology
Psychiatry/Psychology
Pulmonary/Respiratory Diseases
Rheumatology