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Medical affairs in Pharma are often seen as a central agency that works within a healthcare company and prioritize communication among life science organizations, medical professionals, healthcare providers, and patients. Its primary function is communicating scientific and clinical information to the medical community through various channels.
These medical affairs teams derive their value from high-profile medical expertise and provide efficient evidence of pharmaceutical products and medical devices. Team experts also impart details related to educational opportunities to healthcare aspirants and improve their qualifications for eligibility to enter medical affairs teams.
Moreover, the educators of medical affairs instruct healthcare professionals through their scientific knowledge and clinical experience.
A medical affair is a pharmaceutical or medical company department that communicates the correct information about the drug or medical device to doctors, other medical practitioners and healthcare providers.
For instance, medical affairs instruct the applications of a drug to potential healthcare companies after going through clinical cases. Medical affairs definition uses clinical and scientific information to communicate the efficiency of a drug.
The pharmaceutical medical affairs department officials include professionals with masters or doctorate degrees in pharmaceuticals. They instruct the applications of a drug to potential healthcare subscribers as soon as it is circulated in the market. They describe its use through a scientific and clinical approach by means of medical science liaisons. That is why the personnel working in medical affairs departments are known to be experts and leaders in the medical science field.
They provide information about the following:
Independent medical education
Under its internal affairs, the pharmaceutical ones bring together the research and commercial wings of the pharma businesses. Medical affairs teams analyze and translate important details on therapeutics and drugs into an easy language for better understanding. Any healthcare experts and sales representatives can then grasp these details without a scientific background.
There are also additional responsibilities of these teams, which include:
Conducting non-registered clinical trials after the FDA approval of a drug.
They also execute drug outcome studies and support healthcare brands.
The department of medical affairs encompasses an array of roles and responsibilities. It has to act as a bridge between medical scientists and healthcare product manufacturers.
The officials of medical affairs departments are increasingly playing the central role of creating coordination among the internal teams for attributes such as commercial, market access, regulatory, clinical development, implementation, and drug safety.
These teams clearly convey their concerns about the company data and consistently educate on it. Besides these regular pharma medical affairs, its functions can also cover reorienting preclinical research. For this purpose, marketers create special medical affairs strategies. These strategies aim to facilitate trials that investigators initiate based on their predefined areas of interest.
These strategies would enable the identification of new targets. It will also facilitate accessible developments in future clinical trials future clinical and increase knowledge about patients.
Medical affairs experts represent pharmaceutical companies and facilitate them in maintaining the flow of information within the medical communities. During their interactions, these communities learn about a particular healthcare product’s market status.
The following are the main functions of medical affairs in pharmaceutical industries:
They undertake the responsibility for additional clinical trials by the professionals of medical affairs that are non-registered.
These officials conduct studies on healthcare economics and outcomes from a drug. This study is done to evaluate the results of using a medicine. The main idea behind the study is to estimate the medical cost of a drug and observe the quality of a patient’s life after using the drug.
Helping the brand team in formulating scientific strategy.
The officials review proposals for clinical trials that independent investigators prepare.
Defining a publication plan for each product and coordinating clinical and scientific communication at medical conferences rests with the medical affairs team.
Medical affairs professionals nurture relationships with key stakeholders such as healthcare practitioners and academic researchers.
Sponsoring healthcare practitioners’ education programs was in pharma medical affairs’ hands. They support the internal training programs.
The medical affairs team is almost like any other industry vertical PR team. They are abreast with the latest happenings within the industry, not just of their organization but of their competitors too.
Today, medical affairs teams hold great significance within pharmaceutical businesses. They are marking their presence felt due to their collaborative characters.
These teams are much more collaborative than working in isolation, allowing their expertise to have a wider impact within the medical fraternity. New medical affairs employment opportunities are also rising, indicating a revolution in pharmaceutical industries.
For example, an increasing number of medical sales liaisons in the industry are shaping pharmaceutical companies perfectly enough to remain at the edge of the competition and highly advanced in the upcoming novel treatments.
The medical affairs team’s contribution has a far-reaching impact on patient care. They are also helping to lead the pharma industry into a new age of scientific development and open collaboration.
Improving medical communication is extremely important for a pharmaceutical company as it needs to translate complex science into layman’s language.
Thus, medical information and communication professionals make use of data and insights and support medical affairs departments for:
Leveraging communicative plans
Managing the publication of new information
Engaging with experts and thought leaders
Providing medical education
Facilitating internal communication
Organizing and managing HCPs events and advisory boards
Many products and devices fail to reach the market because of safety concerns and improper communication. Therefore, it is vital to implement successful medical communication plans throughout the product lifecycle.
These plans are necessary to include the right stakeholders. Ensuring the right stakeholders can lead to adequate scientific dialogue.
Communicating medical information not only involves interacting with external stakeholders and maintaining up-to-date information on medical news. The report additionally includes-
Reviews of a promotional interview
Developments in in-field roles
Creating product launch tool kits
Framing education and training materials
Setting up medical information booths
Preparing conference presentations and posters
Verification of content on product-specific and company-sponsored websites
Organizing clinical trial activities
Several digital channels other than emails and phone calls are emerging for effective communication. Examples of novel digital channels for healthcare systems are-
Social media platforms such as Twitter
Voice search is also an emerging trend among different channels.
These additional means of interaction are expected to expand medical and scientific information transformation with patients and related officers.
The rise of difficult-to-communicate therapies and personalized increased the need for improved communication. It has also become important for success in the pharmaceutical industry.
As a result of these developments, companies are trying to manage contact centers and create accurate response documents effectively.
A deep insight into medical information activities enables companies to shape the treatment journey of their patients. It also helps them to reduce the hurdles that come up in the way of getting marketing approvals.
The companies will also be able to identify new patients for clinical trials and even engage with the right key opinion leaders by analyzing their inquiries, which is undeniable.
Most importantly, they identify trending topics and provide opinions, insights, and metrics to measure content quality usage metrics to reveal the need to address safety, efficiency, or quality issues before the time ends.
Also, they determine the highly impacted areas that focus on the potentiality of medical education, re-training, or product needs (e.g., formulation change).
In recent years, continuous regulatory norms drove the importance of forming medical affairs teams. Many of the responsibilities on the regulatory team have been shifted to medical affairs. Many of the responsibilities include-
Updating policies– Relevant drug and device-related information must be updated regularly to deliver valuable medical information.
Framing training programs- The increased use of MSLs or regional medical liaisons to engage in scientific exchange with healthcare providers requires comprehensive policies and training of sales and marketing employees.
Monitoring MSL employees– As the use of MSLs increases, the compliance issues surrounding these practices increase as well because MSLs must be assessed to ensure they remain compliant with the regulations affecting scientific communication.
Planning the overall budget
Planning the overall budget to contain the development of new therapies and medical devices is another challenge, according to Medical Affairs Resources, Structures & Trends in primary research conducted by Best Practices. Since several therapies are arising, pharmaceutical companies are promising to lead in their transformation. Besides, the departments should also comply with regulatory policies primarily related to the cost of specialty treatments.
The researchers also explained that these advanced treatments are pressuring governments to allocate budgets accurately to new therapies and technologies budgeting.
Medical affairs in the pharmaceutical industry are frequently observed as supporters of companies. That is why responsibilities are increasingly being transferred from the regulatory departments of this department. Its responsibilities also encompass research in the medical field and communicating the data collected among concerned authorities.
We live during times marking the paradigm shift from an environment dominated by commercial and marketing interests towards a new dimension in the advancing medical field. Medical knowledge and patients are being centrally focused along with successfully commercializing the prepared drugs.
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