An India based vertically integrated pharmaceutical company was looking for Freyr’s Regulatory support to prepare non-clinical overviews. The client had to prepare and submit the non-clinical overviews to the Health Authority (MPA), as per the eCTD module 2.4. As the molecule was old and less regulated, there was limited data availability and broad pharmacological class.
Read through the proven case study to understand Freyr’s expedited services to prepare the non-clinical overviews. Download now.
Fill the form below to download the Case Study
