Information Officer
Managing pharmaceutical information and marketing compliance
To be fully compliant with legal requirements, a qualified expert has to take responsibility over how information on pharmaceuticals is communicated and marketed.
Managing your information
How far are pharmaceutical companies allowed to go when advertising their products? Which information must be communicated in a summary of product characteristics?
To be fully compliant with legal requirements, a qualified expert has to take responsibility over how information on pharmaceuticals is communicated and marketed.
Responsibilities of an Information Officer:
• They must have a solid understanding of the medical and scientific field to apply all relevant guidelines appropriately.
• They are responsible for ensuring that labeling, package inserts, product information, and advertising for a product align with its approval or registration.
• They need to create product information, instructions for use, and mandatory text.
• They bear the responsibility for maintaining up-to-date instructions for use, product information, and mandatory text.
• They must stay informed about relevant changes in regulations, laws, and deadlines and implement them accordingly.
• They coordinate with the relevant authorities as needed.
• They conduct training sessions to raise awareness among sales and marketing personnel about applicable legal regulations.
How we support you
Pharmaceutical companies operate within strict legal frameworks when it comes to communicating and marketing their products. To avoid risks and ensure compliance, a qualified Information Officer plays a pivotal role in managing and overseeing all product-related communication. Here's what makes this role indispensable:
Industry expertise
Our team brings years of experience in the pharmaceutical and life sciences sectors, ensuring you receive tailored guidance to meet regulatory expectations.
Comprehensive solutions
We ensure all your materials meet legal requirements, including: Labeling (clear, accurate, and compliant product labels), Patient Information Leaflets (PIL), Summary of Product Characteristics (SmPC), and Advertising materials (fully compliant promotional content).
Empower your team
Through targeted training sessions, we equip your sales and marketing teams with the knowledge to navigate legal boundaries confidently and effectively.
Why QbD Group
Your trusted partner
Choosing QbD Group means partnering with a trusted leader in Regulatory Affairs. With over a decade of expertise, we provide tailored support across the entire product lifecycle, ensuring seamless compliance and customer satisfaction on a global scale.
10+ years of experience: benefit from our team of highly qualified consultants.
Full life cycle support: full support from pre- to the post-marketing phase.
Global presence: QbD Group operates globally, with QbD Austria having a special focus on Europe (EU) and China.
Customer satisfaction: constant evaluation, transparency and clear objectives.
Let's talk Regulatory Affairs
From regulatory strategy to product approval, our experts are ready to guide you through every step.