Health Authority
Meeting Support
Interacting with executive authorities or regulatory health agencies
When it comes to interacting with executive authorities or regulatory health agencies, this is a part of developing a product for companies in the life sciences. Whether you ‘re preparing for a pre-IND NDA with something like the FDA or EMA meetings, BioBoston Consulting is ready to bring its expertise to bear on Health Authority Meeting Support and ensure productive, efficient outcomes for your back-breaking effort.
Customers
We have a team that knows everything there is to know about health authority affairs, regulatory factor monitoring, and helps you get ready.
Staff for Tailoring Your Meeting
BioBoston offers all the support from meeting preparation to management. You will be perfectly poised to deal with key questions.
Advisors in Strategy
As you prepare for a meeting with the agencies, we work closely with you in order to write the desired communication documents, identify key points, and foresee what the regulatory authorities will respond.
Risk Management
We help you mitigate risks by discovering potential regulatory issues early, and planning ways to deal with them during discussions with health authorities.
Expertise on Global Health Authorities
We have been in the regulatory space of multiple decades, and know how regulatory agencies like the FDA, EMA, and others think. Our guidance ensures that your interactions with these organizations are aligned to global regulatory expectations.
Services Bio Boston Consulting Provides
Strategic preparations and planning
We will map out a comprehensive strategy for interacting with health authorities tailored to the stage of your product’s development.
Briefing papers
Making well-prepared briefing papers to explain your development strategy, data and key questions to regulatory authorities.
Analysis of Regulatory Questions
In order to work hard, one must also anticipate and analyze questions or concerns originating from health authorities.
Mock Meetings and Rehearsals before the Real Thing
We will hold these so your team gets a sense of what is expected and how to work with various responses, and blooms with confidence during the actual meeting.
Managing Communication with Health Authorities
This includes ensuring all communications are professional, timely, and in line with your Regulatory strategy.
Post-Meeting Follow-up
We provide a summary, conclusions, and actionable suggestions from the meeting. Pointers will guide the next steps in your product development or Regulatory planning.
BioBoston Consulting Makes Successful Regulatory Meetings Whether health authority tasks are to be in step with or achieve regulatory outcomes, with our Health Authority Meeting Support they will reflect the mood of your product development.
Let Us Support You
Consult us now, Boston Consulting can prepare you for health authority meetings and work together with you on a successful regulatory outcome.
All Services
- Quality Assurance and Regulatory Compliance
- Investigational New Drug (IND) Application
- Regulatory Strategy & Submissions
- Investigational Device Exemption (IDE) Application
- Vendor Selection & Qualification
- Project & Risk Management
- Technology Transfer
- Quality Management Systems (QMS)
- Gap Assessment and Remediation
- Funding and Investment Strategies
- Research and Development (R&D)
- Biostatistics and Data Analysis
- Lab Operations and Efficiency
- Medical Writing
- CDMO Vendor Selection Qualification & Oversight
- CRO Selection & Qualification
- CTO Selection & Qualification
- Data Integrity and Software Implementation
- Clinical Operations
- Clinical Trial Monitoring
- FDA Inspection Readiness
- Internal and Supplier Audits
- Regulatory CMC Support
- Qualification and Validation
- GxP Training
- Computer System Validation (CSV)
- Strategic Advising
- Process Optimization
- Health Authority Meeting Support
- Recruitment