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Pierrel Research

Pierrel Research has more than 20 years of experience as a full-solutions Contract Research Organization (CRO) providing drug development services to the pharmaceutical, biotechnology, and medical device industries.

Solutions across the full spectrum of clinical research and regulatory requirements

Pierrel Resarch has its Global Headquarters in Zurich, Switzerland, with Operational Headquarters in Essen, Germany, Philadelphia, United States, and Saint-Petersburg, Russia.

Their international and highly skilled multidisciplinary teams work to consistently offer high quality and cost effective services and solutions across the full spectrum of clinical research and regulatory requirements.

They offer consultancy services for clinical and regulatory development programs as well as operational services to effectively conduct global Phase I – IV programs, Late Phase, and Non-Interventional Studies (NIS).

Consultancy services for over 80 countries throughout the world

Pierrel Resarch’s clinical staff is strategically located in over 20 offices worldwide, thus enabling a high level of local expertise to be applied to global clinical trials of all sizes. Their regulatory affairs expert network offers consultancy services for over 80 countries throughout the world, resulting in global coverage for your program.

Global locations

They are committed to the application of evolving technology to constantly achieve the highest levels of performance and quality. Pierrel Research is at the leading edge of this technology with HyperSuite®, a state-of-the-art web-based clinical trial management system that is validated and 21 CFR Part 11-compliant.

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More than 18 000 well-established investigational sites from different countries have taken part and been successful in enrolling of more than 170 000 patients during the last two years.

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Clinical Research Solutions

Pierrel Research covers every aspect of clinical research, from First-In-Human through Proof-of-Concept up to complete Phase III- IV international clinical development programs and post-approval projects.

  • International Project Management
  • International Regulatory Advice and Support (Clinic Development Plans)
  • Data Management
  • eClinical Trial-Technology (HyperSuite®)
  • Independent Quality Assurance
  • Biometrics, Psychometrics, Econometrics
  • Pharmacovigilance
  • Early Phase
  • Late Phase
  • Medical Writing
  • IMP Manufacturing
  • Trial Materials / IMP Logistics

Contact

Pierrel Research International AG
Bahnhofstr. 20
P.O. Box 173
8800 Thalwil
Zurich
Switzerland
Tel: +41 44 723 5959
Email: office.global@pierrelgroup.com
URL: www.pierrel-research.com

Biometrics, Psychometrics, Econometrics, ePRO

With one of the largest biostatistical departments in Europe, Pierrel Research offers full service for design and methodology within clinical trials.

Different expertise and backgrounds form a creative mixture and the basis for constructive and client-oriented statistical work.Beyond the standard biostatistical work, we offer highly sophisticated methodologies such as adaptive designs, psychometrics including scale development, population pharmacokinetics, meta-analysis, overall safety analyses and others.Planning:Parallel Group DesignCross-over DesignFactorial DesignMulticentre TrialsSuperiority TrialsNon Inferiority/Equivalence TrialsDose-Response DesignsGroup Sequential DesignsSample size determination…

Data Management

High-speed networks and high-capacity servers guarantee smooth data processing and data storage at all points during the project life cycle

We customize software according to our clients' needs state-of-the- art. To comply with our customers' requirements, Pierrel Research offers study data storage in both, SAS or Oracle.The state-of-the-art double-data entry with audit trail and CRF-tracking (pCRF or eCRF) as well as the query management system based on a fully validated (21 CFR part 11-compliant) web-based…

Early Phase

Pierrel Research offers clinical pharmacology services in three Phase I Units located in Romania. Their experts warrant that studies are carried out safely and effectively in accordance to GCP.

Pierrel Research offers clinical pharmacology services in three Phase I Units located in Romania (Timisoara and Arad). An interdisciplinary team of experts warrants that studies are carried out safely and effectively in accordance to Good Clinical Practice (GCP) requirements for a wide range of research fields.Pierrel Research provides professionally conducted human Phase I, early Phase…

eClinical Trial-Technology (HyperSuite®)

In addition to expertise in conducting of clinical trials, Pierrel Research offers a strong understanding of e-clinical trial technologies. The deep knowledge of our experts on the design, implementation and validation of clinical trial technology solutions and our large and proven practice experience cooperating with the clinical teams ensure tailored made solutions to our clients.

Through our state-of-the-art internet technology (HyperSuite®), we are able to provide innovative e-clinical trial services to speed up, increase the quality and streamline the data handling processes, facilitate project management and save costs.Pierrel Research's combination of clinical and technological expertise helps clients find better ways to conduct clinical research, and ultimately, to rapidly bring safely…

International IMP Services

International IMP Services, a specialized company within Pierrel Research group, is proud to provide high quality Investigational Medicinal Product (IMP) services for international clinical trials.

Services include contract IMP manufacture (packaging, labelling, certification by a QP in accordance with Directive 2001/20/EC) and IMP logistics tailored to meet the specific requirements of Phase I through Phase IV clinical trials.We are a leading global provider of clinical trial services combining more than 20 years of experience in the planning and conduct of…

Medical Writing

Regardless of your product study phase, our highly skilled medical writers can save you time and costs by clearly and accurately writing the medical documents your development program requires. We will provide you with thoughtful, cohesive medical documents that will stand up to regulatory and industry scrutiny.

Below are examples of the various medical documents we routinely write:Trial synopses, protocols and amendmentsPatient information sheets & informed consent formsCase report form (CRF) designPatient questionnaires & diariesInvestigator BrochuresStandard operating procedures (SOPs )Summary of clinical safety/ISSIntegrated summary of efficacy (ISE) reportsNon-clinical pharmacology and toxicologyBenefit-risk analysesIntegrated clinical trial reports (ICH E3) / interim reportsCommon Technical Documents…

Pharmacovigilance

Pierrel Research offers a comprehensive portfolio of services for the active management of product safety and patient health during the entire lifecycle of a product, helping you manage your pre- and post-marketed product safety program.

Our global reach, quality system approach, leading technology for SAE and AE cases management and reporting, combined with a multi-disciplinary safety expertise offers true value and key benefits to pharma, biotech and device companies.Pierrel Research is your strategic partner with specific product safety expertise who can minimize your current cost pressure while unlocking value and…
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Quick Contact Pierrel Research
Quick Contact Pierrel Research


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