BoosConsulting - Pharmacovigilance | Pharma Law
Do these or similar situations sound familiar to you?
● Do you have too much work and too few staff?
● Do vacation time, illness, parental leave jeopardize deadlines?
● Does an ad-hoc request from an authority (EMA/BfArM) lead to short-term bottlenecks?
● Does a change in personnel is cause temporary capacity problems?
● Are requested internal resources not approved?
● Have new regulatory requirements to be implemented once again?
● Is an inspection/audit coming up?
BoosConsulting supports pharma and biotech companies by temporarily providing qualified personnel or specific know-how (e.g. for implementing regulatory requirements), particularly in the area of pharmacovigilance (drug safety, patient safety).
With BoosConsulting, you have an external resource at your disposal that knows these challenges from first-hand experience and - with 20+ years of practice in the healthcare industry - can provide fast, targeted and tailored solutions.
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So that
compliance with regulatory requirements
is ensured, authority
deadlines
are met and the workload of you and your team gets noticeably
reduced.
What services does BoosConsulting offer?
BoosConsulting specialises in the following areas:
Based on 20+ years of solid experience in this field, a special focus is on pharmacovigilance (drug safety / drug surveillance / patient safety) is the key focus of activities.
Beyond the pharmacovigilance core business, particular services on medical devices and pharmaceutical law matters are covered.
NOW NEW: TUEV-certified AI Compliance Officer
Effective and efficient collaboration for your objectives:
Whether consulting, interim management, specialised services, outsourcing or another form of cooperation - BoosConsulting has the right individual solution for you.
Your direct route to qualified support:
