Profile

Profile

Founded by Dr Dima Al-Hadithi in 2013, Minaret Consulting Ltd offers you a broad range of pharmaceutical regulatory services supporting drug development through to post licensing activities.

As an ex-MHRA assessor and EMA quality expert , I pride myself on delivering open and honest communication, underpinned by integrity and sound technical knowledge.

Whether you are working with an innovator product, an Over-the-Counter (OTC) product or a generic, I can help light the pathway through the regulatory maze.

Your success is our success.

Services

At Minaret Consulting, we offer regulatory expertise and project management services. Some of these services are listed below and we are always happy to explore your needs whether small or large. We also work with fellow industry and ex-regulator experts to offer a single solution to your regulatory requirements.

Licensing

From clinical development to licensing through to post-approval variations

Technical Expertise

Chemistry, Manufacturing, Controls (CMC) aspects in the submission dossier: data requirements, CTD authoring, data review

Project Management

Full project management of technical transfers and remediation projects

Regulatory Compliance

Performing GAP analysis to measure your existing license against manufacturing and testing protocols

Custom Training

Provision of tailored training to maximise the potential of your teams

Experience

Please click on the linked-in icon to view my career history and experience.
Dr Dima Al-Hadithi
Dr Dima Al-Hadithi
BPharm, MRPharmS, PhD, MTopra

"Product launch dates and costs are key factors and we help you to determine how to achieve the best outcome with patient safety in mind. We help you to build quality in to your product and systems to stay compliant"

Latest news