- Drafted and advised on clinical trial agreements and legal representative agreements, also providing specific advice in relation to the responsibility assumed and protection required for legal representatives in clinical trials.
- On-site compliance audit of several pharmaceutical companies in respect of marketing and advertising practices.
- Drafted standard operating policies in respect of marketing and advertising practices.
- Advised on advertising and marketing policies considering the ABPI Code and the Blue Book.
- Advised on generic entries into the market and submissions to the EMEA and European Commission regarding serious public health concerns of generic products.
- Due diligence for several companies in respect of the prospective acquisitions of medicinal products.