Services

BMA offers a wide range of support services to the pharmaceutical, biotechnology, and medical device industries. We have partnered with leading companies to successfully complete clinical studies with the highest level of compliance. Our highly customizable team and services can be modified quickly to help you achieve your goals. We have the capabilities and knowledge to expand our services based upon your requirements. 

You have a choice when outsourcing your project. Let the team at BMA diligently and professionally manage all of your clinical trial needs.

Learn more about our services and how you can get the most out of your study and internal resources by partnering with BMA.


Study Management

• Feasibility and Site Selection Activities
• Initial Regulatory Packet Preparation and Dissemination
• Regulatory and Financial Document Creation, Collection, Review, and Maintenance
• Study Contract and Patient Budget Negotiations
• Tracking, Collating, and Follow-up of Vendor and Study Data
• Informed Consent Creation, Review & Maintenance
• Safety Information and Study Correspondence Distribution
• Regulatory File Audit and FDA Submission Support
• Drug and Biologics Temperature Monitoring (Cold Chain)
• Clinical Study Manager Responsibilities

 Study Management Overview

Data Management

• Data Discrepancy Management
• Post-Study Follow-up
• Clinical Scientist Support
  

 Data Management

Clinical Monitoring

• Clinical Monitoring

 Clinical Monitoring

Project Management

• Project Management

B. Mclaughlin Associates, Inc.

 BMA Overview