Our Company

 Convex Clinical Research Services

 

 

 Convex Clinical Research Center

 

 Convex Ltd. is a local CRO, which partners with leading pharmaceutical,

biotechnology and medical device companies. The majority of our clients

are international medium- to large-sized CROs. As a full-service Clinical

Research Organization, we combine efficient clinical trial management,

comprehensive regulatory consulting and know-how to create a customized

approach that ensures higher quality services for our international partners.

Over the past two decades, Convex has completed over 243 clinical trials in

various therapeutic areas. We offer flexible service models ranging from

 

 Convex Clinical Research Center was founded

in 2015 to provide therapeutic expertise to the

pharmaceutical and biotechnology industries across

a range of services. The CRC is dedicated to the

conduct of early-phase clinical pharmacology studies

in healthy volunteers, and patient populations over a

spectrum of diseases. The CRC is a fully owned subsidiary

of Convex Ltd. and is fully integrated with Convex CRO.

                                                

 

    

 

full-service packages to specific functional service options. Convex's currently

active clients come from Italy, France, Germany, US, Poland and Israel. Our

commitment to quality and continuous innovation has created long-lasting client

relationships. Convex provides all in-country’ clinical trial services from feasibility

to the finalend-of-study regulatory submission. No matter what your study design

is we meet all requirements on time and on budget. For the excellent performance

to every protocol we provide:

 

  • Feasibility Manager
  • Contract Negotiation Specialists
  • Medical Writing Specialist
  • Clinical Study Manager
  • Study Subject Recruitment Specialist
  • Well-trained CRAs and CTAs
  • Data Management Specialist
  • Biostatistic specialist

 

Our services include:

 

  • Study Feasibilities
  • Strategy Consultation
  • Sites Selection
  • Medical Writing
  • Regulatory and Ethics Submissions
  • Site and Investigator Contract Negotiations
  • Investigator Meeting Organization
  • All monitoring and Study Oversight
  • Project Management
  • Clinical Study Supplies Provisioning
  • Data Management
  • Biostatistical Analysis
  • PK Evaluation
 

We believe this provides our partners with many advantages.

The site conducts phase I-IV clinical trials annually in a variety

of therapeutic indications, involving patient populations and healthy

volunteers. Our expertise:

 

  • Early phase studies
  • Dose ranging, single/multiple
  • Bioavailability/Bioequivalence
  • Pharmacokinetics
  • Pharmacodynamics
  • Drug/Drug Interaction
  • Drug and food interaction
  • Blind dosing/sampling
  • Food effect studies
  • Multiple dose studies
  • Vaccine studies
  • Food supplement studies
  • Medical devices studies

 

Our headquarter is located within 3 kilometers of our CRC

allowing for productive face to face team meetings supporting

more efficient communication, cost savings and seamless study

execution between the CRO and CRO services. We expedite study

recruitment by pre-screening potential subjects from our database

by querying against the study inclusion/exclusion criteria.