Clinical Data Management – the process of collection, cleaning, and management of subject data in compliance with regulatory standards.Data Management...
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All drug development procedures involve dealing with voluminous documentation which must include consistent, reliable and accurate data. For this reas...
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This is a training the aims to help you understand the principles behind what is considered Ethical when it comes to Clinical Research. It is based on...
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Every clinical research begins with the development of a clinical protocol. What is really important is for the protocol to be in absolute compliance ...
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Free Good Laboratory Practices (GLP) is linked to a quality system that controls how non-clinical safety studies are planned, conducted, monitored, re...
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This completely FREE Good Manufacturing Practices (GMP) Training provides access to the GMP guidelines in a well-structured and user friendly way and ...
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The training is focused on the most important aspects of GCP Inspections - what are the more important findings and what are the consequences from the...
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This training is based on the international regulations for Good Distribution Practice (GDP) of pharmaceutical products for human use. The training lo...
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GSP demonstrates that pharmaceutical companies are dedicated to quality in every aspect of their services provided to patients and the industry as a w...
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This is a short guide that presents all the main regulations and steps that a company/individual should know and make in order to be approved legally ...
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Clinical Data Management – the process of collection, cleaning, and management of subject data in compliance with regulatory standards.Data Management is a very crucial aspect of clinical research, explaining its burst in popularity and the pinned fo...
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All drug development procedures involve dealing with voluminous documentation which must include consistent, reliable and accurate data. For this reason, effective data management planning is essential to clinical studies and their appropriate conduc...
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This is a training the aims to help you understand the principles behind what is considered Ethical when it comes to Clinical Research. It is based on the ICH standards and specifically focuses on studies, involving Human subjects, but is not limited...
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Every clinical research begins with the development of a clinical protocol. What is really important is for the protocol to be in absolute compliance with regulatory/GCP requirements. Astra Nova’s Following the Protocol training emphasizes on the sig...
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Free Good Laboratory Practices (GLP) is linked to a quality system that controls how non-clinical safety studies are planned, conducted, monitored, recorded, reported, documented and archived. This course is useful for those who work in a GLP regulat...
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This completely FREE Good Manufacturing Practices (GMP) Training provides access to the GMP guidelines in a well-structured and user friendly way and reads theInternational GMP regulations, which have been adopted by local legislation worldwide. This...
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The training is focused on the most important aspects of GCP Inspections - what are the more important findings and what are the consequences from them, how are inspection findings categorised and how do they relate to the benefit-risk evaluation....
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This training is based on the international regulations for Good Distribution Practice (GDP) of pharmaceutical products for human use. The training looks into the practices of wholesale distributors and the proper ways and processes concerning the di...
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GSP demonstrates that pharmaceutical companies are dedicated to quality in every aspect of their services provided to patients and the industry as a whole. Therefore, our training offers a thorough introduction to Good Storage Practices for the pharm...
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This is a short guide that presents all the main regulations and steps that a company/individual should know and make in order to be approved legally as a wholesale dealer. The approval comes with a license on behalf of the local institution but only...
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