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grapl

grapl is a UK based digital learning and development specialist, authoring and designing ZenosisĀ® courses to provide an extensive eLearning library for the pharmaceutical, biotech and medicinal products sector. This learning can be delivered via the customers LMS, the grapl LMS or its social, knowledge and collaborative CloudRooms platform. Continuously updated to reflect regulatory changes, ZenosisĀ® courses are trusted to educate their people by some of the worlds leading companies. 

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CPD Courses & Workshops

Education

An Introduction to Drug Safety and Pharmacovigilan...

grapl

Drug safety monitoring and risk management are vitally important for medicinal product developers; l...
Online Course
Education

An Introduction to Clinical Trials and Drug Develo...

grapl

This course provides an understanding of how clinical trials fit into the drug development process....
Online Course
Education

An Introduction to Clinical Trial Preparation and...

grapl

Worldwide expenditure on R&D by the pharmaceutical industry is continually increasing. Most of the f...
Online Course
Education

ICH Good Clinical Practice

grapl

Good Clinical Practice (GCP) is a set of internationally recognised ethical and scientific quality r...
Online Course
Education

An Introduction to Good Manufacturing Practice for...

grapl

Everyone who works in a processing; quality control; packaging; or warehouse environment for a pharm...
Online Course
Education

Essentials of EU and US Regulatory Affairs for Hum...

grapl

This foundation-level module is the ideal introduction for new entrants to the field of pharmaceutic...
Online Course
Education

The Investigational New Drug Application (IND) to...

grapl

An Investigational New Drug Application (IND) is a submission to the US Food and Drug Administration...
Online Course
Education

Good Documentation Practice

grapl

Good Manufacturing Practice (GMP) for medicinal products relies on documentation. Good Documentation...
Online Course
Education

Good Manufacturing Practice in Cleaning and Sanita...

grapl

Cleaning and sanitation of premises and equipment are essential to efforts to prevent contamination...
Online Course
Education

Good Manufacturing Practice for the Warehouse

grapl

This module explains the requirements of Good Manufacturing Practice (GMP) for the warehouse; and ho...
Online Course
Education

Good Manufacturing Practice in Processing Medicina...

grapl

Operations in the dispensary and on processing lines are at the heart of medicinal product manufactu...
Online Course
Education

Good Manufacturing Practice in Packaging Medicinal...

grapl

Packaging operations constitute the last manufacturing step before release of a product to the marke...
Online Course
Education

Corrective and Preventive Action (CAPA) in Medicin...

grapl

A company’s Corrective and Preventive Action (CAPA) system establishes how personnel should deal wit...
Online Course
Education

Risk Management Planning for Medicinal Products

grapl

Proactive risk management is a major component of good pharmacovigilance practice. This module sets...
Online Course
Education

Signal Detection and Management in Pharmacovigilan...

grapl

Product licence holders and regulatory authorities monitor the safety of licensed drugs to detect ad...
Online Course
Education

Urgent Safety Restrictions

grapl

An Urgent Safety Restriction (USR) is a regulatory action taken in response to a safety signal to ma...
Online Course
Education

Good Pharmacoepidemiology Practice

grapl

Pharmacoepidemiology is the study of the use and effects of drugs in large numbers of people. It pro...
Online Course
Education

Clinical Trial Monitoring: Study Monitoring; Docum...

grapl

The sponsor of a clinical trial must arrange for it to be monitored throughout its duration to ensur...
Online Course
Education

Clinical Trial Monitoring: Site Evaluation and Set...

grapl

The sponsor of a clinical trial needs to reach agreement with clinical investigators to conduct the...
Online Course
Education

How to Gain and Maintain Approval for Clinical Res...

grapl

To conduct a clinical trial in the European Economic Area under the Clinical Trials Directive the sp...
Online Course
Education

Good Clinical Practice Inspections and Audits

grapl

Good Clinical Practice (GCP) inspections and audits are carried out to provide assurance that: the r...
Online Course
Education

How to Gain Authorisation for Clinical Research un...

grapl

To conduct a clinical trial in one or more member states of the European Economic Area (EEA) a spons...
Online Course
Education

How to Conduct Clinical Research under the EU Clin...

grapl

This course describes the requirements that must be met by; and options available to; the sponsor du...
Online Course
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