As an experienced regulatory compliance expert, I have successfully completed 1370+ legal projects, many of which have been centered around litigation, contracts, and patents - all areas that demand immense attention to detail and in-depth understanding of key compliance standards. I have successfully designed and implemented comprehensive legal strategies for my clients time and again. This exposure has equipped me with familiarity on FDA guidelines (GMP, GLP, GCP) as well as industry standards (ISO 13485, ISO 9001, ICH guidelines) which clearly resonates with your project needs.
Importantly, my training as a lawyer emphasizes on critical thinking and problem-solving skills which are paramount to evaluating quality systems, identifying gaps and potential pitfalls in compliance. Additionally, my work involves frequent communication with clients, brainstorming actions and mitigation plans ensuring total confidentiality of sensitive information – a skill that is highly pivotal to conducting rigorous mock FDA audits.
Moreover, my postgraduate certification on intellectual property rights from University of Pennsylvania coupled with my experience in Nano particles and calcium phosphate further comes into play harmoniously in the pharmaceutical sector. All in all, you can trust me to seamlessly manage your project ensuring effective communication with all stakeholders while delivering tailored strategies meticulously prepared to keep your organization compliant at all times.