Alliance Drug Development
Alliance Drug Development is a consultancy-based organization, we have been delivering drug development services for over a decade with a team of hand-picked professionals who are subject matter experts in their respective fields. We are based in United Kingdom and Asia.
Within Europe we have helped in all aspects of clinical development through a nimble and effective team comprising of experienced professionals. We have worked with biotech organizations to provide feasibility, CRO selection, site selection, training of in house and hospital staff as well as assisted them in IND applications as well as final reporting of clinical trial and NDA. We have also worked with large pharmaceutical organization on ad-hoc as well as long term projects. Optimizing CRO, by reviewing the plans such as data management, medical monitoring, and statistical analysis. Our review resulted in a SMART plan and helped the organization to receive the service they actually wanted from the CRO.
We have experts and cater for global submissions and have also undertaken niche projects within Pakistan. We have trained and retained several Key Opinion Leaders within Pakistan and can provide access to treatment naïve patients. One of the advantages of using Pakistan for any clinical trial is extremely co-operative Principal Investigators as well as trial staff. Since English is the primary language in medicine; the only document that needs to be translated in Informed Consent form; all other Clinical Trial Documents can be submitted in English.
Our Mission statement
To provide effective and agile drug development service which leads to quick drug development and minimize the questions.
We listen to our clients needs; absorb the information, take time to think and plan and this results in a coherent project with no surprised and lessen any needs of post initiation modifications which are expensive and cause delays. Being able to tap resources from experts in the field we can usually achieve all this in matter of days compared to weeks.
With the diverse background of our consultants, we are able to conceptualize and recommend a tailor made solution which saves time without compromising quality.
Contact Us
Our Services
We cater for all aspects of drug development, from application to approval. We can plan your drug development project from first human trial to the approval of marketing authorization.
Sponsor Medical Oversight
Our team of consultants have been providing medical oversight for sponsors of Clinical Trials. According to current regulations the sponsor is ultimately responsible for the conduct and reporting of trials (SI 2004/1031 Regulation 3).
Clinical Trial Management
We are experienced and have been providing clinical trial management services to biotech as well as pharmaceutical organizations. We have established network with Key Opinion Leaders in Europe and Pakistan
Regulatory Submission
We have access to an expert regulatory team, who are agile and efficient and can develop regulatory strategy with you depending on the objectives, our team has successfully led several IND and NDAs in all major markets.
Regulatory Inspection
Over the past few years, we have undertaken several projects to make the organization ready for inspection. Our motto has always been to be inspection ready all the time.
Training and Development
With access to therapy area experts as well as professionals from all the specialties within clinical research, we can tailor training and development for all levels of your staff.
CRO Optimization
Over the past decade the CROs have become extremely big organizations and with the ICH’s focus on Sponsor Oversight it has become very important for every Biotech organization to make sure that they are compliant with the regulations and guidelines.
Happy Stories
Ut enim ad minim veniam, quis nostrud exercitation ullamco laboris nisi ut aliquip ex ea commodo consequat. Duis aute irure dolor in reprehenderit in voluptate.
Evelyn Jimenez
Debra Peters
Neque porro quisquam est, qui dolorem ipsum quia dolor sit amet, consectetur, adipisci velit, sed quia non numquam eius modi.