Joe Stroll Cartoon SLIMMER me! Joe Stroll

Who’s Joe Stroll?

About Us

Ever wonder how medical products like Advil, Rogaine, Slim Fast, DDI-DDC, and the plethora of blockbuster offerings received market approval?

Medi-Temps, USA, LLC, a division of J. Stroll Associates, Inc. has been serving the Health Life Science Industry since 1968 with quality Physicians, Doctors of Science, Clinical Research Associates, Preclinical, Regulatory, QA/QC and Product Development personnel for special projects.

Well these companies took the most important step to success! They called the highly respected leader in the pharmaceutical and biotech industry. They called “Medi-Temps, USA, LLC!”

Since 1955, J. Stroll Associates, Inc. serves the Biotechnology, Pharmaceutical and Life Science Industries by placing highly experienced and qualified Physicians and Doctorates, Clinical Research, Preclinical, Regulatory, Quality Assurance, Quality Control and Product Development personnel.

More about Medi-Temps, USA, LLC

Our expert consultants are available for weekly or monthly tours. They can telecommute or be on site for your projects.

Our mission is to provide you with a comprehensive choice of the most outstanding, highly qualified candidates to meet your organization’s needs.

We boast over sixty years of experience in service to a broad range of industries:

Fleet services
Financial Services
Medical Devices

And many others

Some of our specialists include:

Doctors of Veterinarian Medicine
IT Specialists
And much more

FACING THE FDA? YOU NEED J. STROLL ASSOCIATES for full time permanent or for temps call Medi-Temps, USA, LLC!

Stroll Associates gives you a critical edge when you are preparing to defend your studies to the FDA. We are the prevention for a negative response.
Stroll Associates will find you a specialist with proven track record to assist your team for a successful NDA. Our specialists are experts who take tittering programs and bring them onto sound ground. Our specialists consistently earn an “overwhelming approval status” from the FDA.
Our candidates and consultants provide design, proof of concept, and implementation of phase I-IV clinical studies. We even have translational medicine specialists ready to assist you. What else do we offer?

Specialists experienced in medical safety reviews for EMEA pediatric submissions.
Experts who perform technology and pharmacoeconomic assessments.
Experienced, qualified medical writers for sections of IND, NDA, and BLA applications. Some were medical reviewers for clinical trials!
Our industry experienced candidates have prepared manuscripts, abstracts and medical/clinical presentations before peer and regulatory agencies.
Professionals with experience in investigator meetings and working knowledge from extensive interactions with KOLs.
Our industry experts possess extensive experience from their interactions with sales and marketing departments. Some successfully developed the creation of medical/clinical databases for major pharmaceutical companies. Some, had major roles in clinical development or held top executive positions in the pharmaceutical & biotechnology industry.

Our candidates are concise, confidential and thorough in their pursuit of excellence. They will help contribute to your bottom line.

If you are not familiar with our company, we are anxious to hear from you about your needs. We will match your requirements with our extensive personnel base to provide you the right candidate at the earliest opportunity.


MediTemps USA Consultancy is offered on a Project Basis, serving the industry since 1968!

Warmest regards,


The Medi-Temps Team!