We help Pharma businesses to anticipate common regulatory Pitfalls & deficiencies.
To support Pharma businesses to accelerate patients’ access to high quality, safe, effective, and affordable medicines while maximizing sustainable annual financial returns for stakeholders.
We know that a vital commercial and strategic objective for Pharma companies is to accelerate patients’ access to high quality, safe, effective medicines, while maximising sustainable financial returns for stakeholders.
Ahadrika Pharma - Servces
Ahadrika Pharma Specialises in the following services
We help to ensure compliance with regulatory requirements related to the development, manufacturing and evaluation of medicinal products ensuring that products meet applicable regulations, standards, and guidelines established by regulatory authorities.
Regulatory Intelligence
We help to monitor and interpret regulatory changes at national and international levels, and to identify potential risks and opportunities associated with these changes.
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Regulatory Affairs
We help to ensure compliance with regulatory requirements relating to the development, registration and lifecycle management of medicines in Africa.
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Scientific & medical writing
We help with the drafting, reviewing, updating or full writing of scientific, clinical and Quality Assurance (QA) documents to support regulatory submissions.
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Regulatory Intelligence
Regulatory Affairs
Scientific & medical writing
Frequently Asked Questions
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Please contact us at info@ahadrikapharma.com and our team will get back to you as soon as possible.
A Non-Disclosure Agreement and Service Level Agreement needs to be signed before rendering the service.
Please contact us for any other service you may require.
For Us, it is not "We can’t do that”, but rather “How can we get it done?.
To be the leading global and trusted partner of effective pharma regulatory affairs intelligence, strategic, innovative, and scientific solutions to accelerate formulation development, regulatory submissions, and approvals, and patients’ access to quality, safe and effective medicines.
To support Pharma businesses to accelerate patients’ access to high quality, safe, effective, and affordable medicines while maximizing sustainable annual financial returns for stakeholders, through reduction of turnaround times for new medicines development and registration, reformulation and approval of variation and renewal applications for registered medicines.