welcome to optimed research, ltd

research for yourself & for future generations

Optimed’s Medical Director, Dr. Donald McNeil, opened the doors of Optimed in 1999 with our first infusion trial.

Since then, we have participated in over 1000 clinical trials and have grown our network to over 30 sites. Optimed’s network of sites span the country from Hawaii to New Jersey in a vast range of therapeutic areas. We have worked with virtually all institutional review boards, central labs and central patient recruitment vendors. We leverage the use of intuitive e-source and e-regulatory systems to allow for remote management of documents.

 

Optimed’s Site Support Model exceeds industry standard metrics for Budget & Contract turn-around time,
Regulatory Start-Up, and IRB submission timelines.

Budget & Contract Turn-Around Time: 72 hours
Regulatory Start-Up: 5 days
IRB Submission Timeline: 48 hours
 

The leaders at Optimed understand what the Sponsors and CROs need to take drugs to market with the least resistance.

Fast start-up times
Hitting enrollment goals
Clean and compliant data
 
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Our Columbus Site Includes the Following:

 
  • Programmable infusion pumps

  • Subject exam rooms

  • Conference room

  • Dedicated space for clinical research associates

  • An emergency cart with automated external defibrillator

  • Daily UPS and FedEx pickup with UPS and FedEx drop boxes on-site.

  • Dry ice access with on-site dry ice freezer storage

  • Copier, scanner, and fax machine

  • Wi-Fi internet access

  • Annual calibration for all equipment

  • Beverages and snacks for subjects

  • An incubator

  • An on-site processing laboratory

  • A -20 degree C freezer, a -70 degree C freezer, and a 2-8 degree C refrigerator

  • A drug storage room that is secured by double lock and contains individual storage cabinets.

  • SONICU temperature monitoring system for drug storage room, freezers, and refrigerator

  • Temperature-controlling systems for the drug storage room

  • IQ Panel security system for our suite

  • Two ambient centrifuges and one ambient/refrigerated combo centrifuge

  • Automatic blood pressure cuffs

  • 12-lead EKG machine

  • A pulmonary function testing machine

 
 

Our physicians at our sites offer niche populations with a robust patient database.

We support our physician’s and encourage them to build a positive reputation in their community for clinical trial research.
At Optimed, we have a hard fast rule that the first study patient is screened within 7 days of activation.
Our Data Team at Optimed are experienced research professionals. Our Data Manager oversees the whole quality process which include the following:

Source to EDC entry within 3-5 days of the visit
Randomization checks (thorough medical record review prior to Randomization)
Pre-IMV Audits (Optimed’s goal is to keep error rates below 2-5% when Monitor comes onsite)
Query resolution

 let’s get in touch! we look forward to hearing from you.