Clinical Supply Chain Management

Clinical Supply Chain Management Follow-up

Ensuring Uninterrupted Supply during Clinical Trials

Clinical supply chain leaders face a variety of planning and execution challenges to ensure a successful clinical trial, such as:

Regulatory requirements

Clinical uncertainties

Logistical constraints around new points of patient care

User acceptance testing for IRT/RTSM

Every challenge needs to be managed effectively and efficiently with no impact on quality and compliance.

Our experts can help you stay focused on patient outcomes through the development of reliable and scalable clinical supply. We understand the risks, volatility, and complexity of moving from preclinical experiments to managing clinical supplies.

The Converge approach combines sound strategy and reliable operations with flawless execution.

What Converge Offers

Supply Chain Strategy

Selection of CDMO, Pack & Label, and Logistics providers

Ancillaries/Comparator sourcing

Packaging configuration & label design

Drug distribution network

Clinical Supply Planning

Manufacturing and primary & secondary packaging

Inventory management

S&OP

Day-to-Day Execution

Management of CDMO, Pack & Label, and Logistics providers

IRT oversight

Inventory management and replenishment for depots & clinical sites

Compliance Infrastructure

Manufacturing & Supply SOPs

Clinical SOPs

Pharmacy Manual

Critical Support Technology

MRP & Supply Planning Tools

IRT/RTSM Selection, Design, Setup & Testing

What Our Clients Say

Thank you all for your tremendous efforts over the year that you have applied in this positive transformation with clinical supply. Your hard work and dedication have truly paid off in more ways that go way beyond ensuring supply alone. Again – a heartfelt THANK YOU! You all are truly AWESOME to work with.

VP, Global Supply Chain, Global Biopharmaceutical Company

When I had to operationalize a complex global FIH study with short expiry IP and multiple depots, I knew it was time to call in an expert! Converge has been wonderful, helping with everything from RFPs for pack and label partners to reviewing IRT specs to planning label strategies and labeling campaigns. I can sleep at night knowing none of my sites will ever run out of drug!

VP, Clinical Operations, Emerging Oncology & Immunology Biotech Company

We engaged with the Converge team to help with a complex clinical supply program for a large global Phase 3 clinical trial. Beyond their professionalism and experience, we found that the Converge team operate as an extension to the sponsor team, working hand-in-hand to achieve ambitious goals. I am happy to report that we met our objectives and delivered a successful trial - the Converge team were very much a part of that success.

Chief Development Officer, Emerging Rare & Infectious Disease Biotech Company

As a small biotech company, we do not have internal resources for all of our needed functions. Working with Converge has been a breath of fresh air since I am confident that our clinical trial supply operations work is in capable hands and being managed by a team that cares about our project as if it is their own company. Working with the knowledgeable, invested, and diligent team members of Converge has taken one thing off of my list of worries in this crazy early biotech environment.

VP, Clinical Operations, Emerging Biotech Company

Running a lean supply chain encountering turnover, we engaged with Converge to support clinical product supply of our pivotal study. They hit the ground running to seamlessly collaborate with all of our study partners and ensure smooth cross boarder distribution, as well as visibility to product expiry and resupply packaging requirements. We were able to maintain a continuous flow of product throughout the study and successfully meet all patient demand.