Pharmaceutical Business review is using cookies

ContinueLearn More
Close

MENE Research

Logo
WHITEPAPERS
Quick Contact MENE Research
Latest Press Release


LATEST VIDEO

MENE Research

MENE RESEARCH is an established Turkish Contract Services Organization, which operates providing high quality services to the pharmaceutical industry.

Combining the advantages of a midsize CRO with local presence and local expertise

MENE Ltd. is established in 2003 and located in Science-park of Gebze Organized Industrial Zone (GOSB), which is recognised as one of the countries most developed and modern organised industrial zones.

MENE Research has a reliable, experienced and qualified team of people from different medical backgrounds who perform in a timely and cost effective manner. Their team has the expertise and the know-how to satisfy the needs of your company/centre/hospital, quickly and professionally.

MENE Research combines the advantages of a midsize CRO with local presence and local expertise. Flexibility, dynamism, personal dedication, simple company structure local knowledge enables MENE Research to offer high value for money services.

International Conference on Harmonization (ICH) compliant

Their clients are local and multinational pharmaceutical companies, medical centres, health funds, doctor’s associations, collaborating CROs, and others.

They also run in compliance with the International Conference on Harmonization (ICH), principles of Good Clinical Practice (GCP) and according with the national, international laws, and business ethics.

MENE Research became the first trials group to be accredited by the country’s Ministry of Health under new trial laws introduced in January, 2009.

MENE Research offers a variety of services, depending on the clients’ needs, some of which are but not limited to:

  • Site Selection and Feasibility
  • Site Management
  • Quality Management
  • Consultancy
  • Regulatory Management
  • Project management
  • EDC
  • Warehouse and Logistics
  • Monitoring
  • Pharmacovigilance
  • Data Management and Statistics
  • Training

Areas of Expertise on Phases include:

Phase I-IV Clinical Trial Management and Monitoring, Feasibilities, site selection, Regulatory Affairs and Operations.

Phase I and Bio-equivalence/Bio-availability studies including: Project management, Study conduct, monitoring, Quality Assurance, Regulatory Affairs activities done directly by MENE.

Volunteer screening, Medical writing, Bio-analytical evaluation, Data Management & Statistics activities conducted with the contracted organization, and studies are conducted by academic personnel, also this unit is certified by Turkish MOH.

Contact

MENE Research Head Office
GOSB Technopark
Kemal Nehrozoglu Cad.
Production Building 2, Unit 1
Gebze, Kocaeli 41480, TURKEY
Tel : (+90 262) 678 88 67
(+90 262) 678 88 68
(+90 262) 751 39 80
Fax: (+90 262) 751 28 38
E-mail: info@meneresearch.com
URL: www.meneresearch.com

Consultancy & Training

Mene Research Expertise Team reviews and provides technical advice to prepare regulatory submissions.

Mene Research expertise group provides tailor made training sessions to sponsors and research institutions.MENE Research provides support to Bioavailability/Bioequivalence (BA/BE) Center which are willing to be inspected by Turkish Ministry of Health (BA/BE Inspection Support). Many companies who look for dedicated staff and full support are already obtaining their approvals with the project management support…

Data Management and Statistics

Mene Research is working with very experienced statisticians in addition to clinical trials of Investigational medicinal products with different needs, local applications, FDA, EMA, medical device etc.

Mene Research is working with very experienced statisticians in addition to clinical trials of Investigational medicinal products with different needs, local applications, FDA, EMA, medical device.DATA MANAGEMENTCRF Design, Development & PrintingCRF TrackingDatabase DesignData EntryData Validation/CleaningQuery ResolutionElectronic Data HandlingMedical Dictionary ManagementMedical CodingSAE ReconciliationQuality ControlDatabase LockSTATISTICSProtocol InputSample Size CalculationPatient RandomizationsAnalysis Plan DevelopmentSAS ProgrammingData ListingsTables, Figures, ListingAnalysis ReportsDSMB…

EDC

MENE EDC combines the innovation and experience of Mene Research in a way that investigators benefit most, enjoying the advantage of one-click menus and easy navigation.

Innovative clinical data collection system developed according to the SAAS model that sees software as a service, On demand, extremely user-friendly for physicians as well as for patients, and with a high degree of customization for our clients (no off-the-shelf software).Custom-developed by senior medically trained personnel and specialized technical experts.Providing you with products starting from…

Monitoring

Swiss BioAnalytics provides bioanalytical services for the DMPK environment. LC-MS analysis for your pharmacokinetic and toxicokinetic preclinical studies as well as for your clinical trials is performed in a GLP compliant environment. We perform all modern sample preparation methods, like solid-phase extraction, liquid-liquid extraction and on-line column switching techniques. The large degree of automation ensures high…

Pharmacovigilance

TAKE - MENE Pharmacovigilance provides the life science industry with strategy, solutions and services for drug safety operations and pharmacovigilance , built on advanced platforms to thereby ensure global regulatory compliance and effective patient safety methodologies.

TAKE's industry leading drug safety framework - SafetyReady™ in association with the regional expertise brought in by Mene Research ensures that customers benefit with highly efficient, proactive and affordable solutions and services to meet global pharmacovigilance needs of sponsor companies, affiliates and agencies.Experienced, high caliber, and well trained professionals.Decades of acquired expertiseWorldwide offices in Europe,…

Project management & Quality Management

Project Manager coordinates the operational aspects of ongoing clinical research organization projects to ensure that the clients’ goals of time, cost, and quality are met. QA group operates independently and conducts internal compliance audits across all the departments for ensuring accuracy and efficiency of your trial.

Mene Research Project Management Group coordinates the operational aspects of ongoing clinical research organization projects to ensure that the clients' goals of time, cost, and quality are met. The Project Manager serves as the primary contact with the client to ensure appropriate communications, project budget management, and meeting of timelines, of targets and of the…

Regulatory Management

Mene Research Regulatory Group efficiently manages and successfully executes all aspects of global start-up according to Sponsor specifications.

Perform quality checks on submission documents and site essential documents; Interact with Authorities, CEC, EC, sites, and international associates;Prepare and approve and adopt to local requirements of informed consent forms;Review pertinent regulations to develop proactive solutions to start-up issues and challenges; and Present during bid defenses, general capabilities meetings, and auditsEnsure that the sections are…

Site Management

Mene SMO resources Clinical Research Coordinators to coordinate with the PI, support, facilitate and coordinate the daily clinical trial activities and play a critical role in the conduct of the study.

Mene SMO able to resourcing The Clinical Research Coordinators (CRC). In order to meet requirements of part-time, full time by sponsor All Mene SMO CRCs are specialized research professional working with and under the direction of the clinical Principal Investigator (PI). While the Principal Investigator is primarily responsible for the overall design, conduct, and management…

Site Selection and Feasibility

Mene Research’s dedicated team helps sponsors identify the right study sites and right investigators by visiting and qualifying investigational sites based on the client’s needs.

Mene Research dedicated team understands if quality sites are selected -- those that meet recruitment goals with targeted number of patients on time, execute the study protocol successfully with qualified and motivated investigators and trial will likely finish on time and yield evaluable data. Choosing a quality site is essential to getting your trial done…

Warehousing and Logistics

Depot Meridian has the ability to handle cold chain and ambient products in its secured temperature controlled and monitored warehouse.

Depot Meridian, a subdivision of MENE Research, is the first inspected and approved clinical trial specific warehouse by the Turkish Ministry of Health.The facility has the ability to handle cold chain and ambient products ranging from IMPs, Medical devices and controlled substances to biological materials in its secured temperature controlled and monitored warehouse. Depot Meridian…
Quick Contact MENE Research
Quick Contact MENE Research
Quick Contact MENE Research


Quick Contact MENE Research
Quick Contact MENE Research
Quick Contact MENE Research


Contact MENE Research

Optional Data

Almost there, complete this form and hit the submit button to complete your registration.

Confirmation

Finally, complete a quick security check and confirm terms and conditions:

Quick Contact MENE Research