- Record: found
- Abstract: not found
- Article: not found
September 2018 EMA/CHMP/BWP/534898/2008 rev. 1 Corrigendum. Committee for Medicinal Products for Human Use (CHMP)—Guideline on the Requirements for Quality Documentation Concerning Biological Investigational Medicinal Products in Clinical Trials
Read this article at
ScienceOpen
There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.