Your strategic regulatory affairs partner for drug registration and license maintenance.
Viuture Medical Consultancy (VMC) has extensive experience in providing regulatory consultancy service to worldwide manufacturers of pharmaceutical products. Our team of experts are seasoned regulatory affairs executives who have spent their careers working in multi-national pharmaceutical companies for more than 10 years.
Our team will access, summarize and assess global regulatory intelligence to ensure submissions are compliant with regional and local requirements. We provide a range of consulting services to help worldwide manufacturers resolve complex regulatory issues.
VMC is here to assist you through a range of regulatory needs. Contact us using the form below to learn more about our industry-leading pharmaceutical regulatory consulting services.
Our Core Service.
Identify latest regulatory requirements
Identify drug classification and registration route in Hong Kong
Develop regulatory strategy
Data gap reviews
Risk assessment
Drug registration and license maintenance (new chemical entity and generic drugs)
In-country representation
Prepare responses to regulatory authorities
Post-submission support
Lifecycle management
Registration process in Hong Kong
Our Step-by-Step Approach to Filing.
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Send us a request: VIUTURE MEDICAL CONSULTANCY LIMITED
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