Sentence examples for requirements of registration from inspiring English sources

The rush to be 'REACH-compliant' to fulfil the minimum requirements of registration of dossiers on schedule and to prepare (e SDS [23, 26] might have led to the submission of incomplete and incorrect registration dossiers and the recommendation of inappropriate RMM.

In accordance with the requirements of registration of biologically active supplements, the DMP has carried out analysis of the quality of the product.

At the committee's legislative drafting session on Tuesday, Representative Paul Kanjorski, the Pennsylvania Democrat who heads the House Financial Services Subcommittee on Capital Markets, added the requirement of registration by offshore funds.

"Engineers operate in many different industries, in government, in research and internationally," so "the need to retrain is constant — continuing professional development is a requirement of registration".

Based on previous research [ 4, 8, 9], we conjecture that the requirement of registration may pose a barrier to accessing the public subsidy.

In the context of our review, the term pharmacogenetics is considered as defined by the International Conference of Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), even if other definitions have been reported in the scientific literature.

This study was conducted in accordance with the guidelines laid down in the International Cooperation of Harmonization of Technical Requirements for Registration of Veterinary Products (VICH) GL9 Good Clinical Practices (GCP) and the European Agency for the evaluation of Medical Products EMEAA).

The trial was conducted in accordance with the Good Clinical Practice Guidelines of the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use, the Declaration of Helsinki and local laws and regulations.

The study was conducted in compliance with Good Clinical Practice (GCP) guidelines of the International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use, the United States Code of Federal Regulations that relate to clinical trial conduct, and the principles of the Declaration of Helsinki.

The study protocols were approved by the institutional review board at each participating site, and both studies were conducted in full compliance with the principles of the International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use, Good Clinical Practice and the Declaration of Helsinki.

Opportunities and challenges of meeting evolving regulatory requirements and compliance standards in a global environment 3.1 Life cycle management of a global product often requires managing multiple specifications required for different countries (International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use, Q12 Concept Paper 2014).