Who we are
Professionals on LinkingPros
Collectively, professionals on LinkingPros outnumbers any healthcare service providing firm or individual consultant, covers more service areas, knows more in all disease areas.
LinkingPros represents a new level of sharing and collaboration!
LinkingPros revolutionises your medical product development lifecycle.
Whether you represent a leading name in the global pharmaceutical market, or just an independent consultant looking to reach out to stakeholders, LinkingPros has got your back.
I represent a pharmaceutical company.
LinkingPros makes it easy and efficient to combine concepts with trials and ship medicines to market.
A wealth of project experience and veteran consultants makes LinkingPros perfect for building experimental healthcare solutions.
Conduct medical trials with confidence and take advantage of LinkingPros library of streamline systems.
I work as an Independent Consultant.
LinkingPros utilises my analytical skills for gathering data on the latest health trends.
LinkingPros helps me create clear, concise reports that communicate recommendations for new healthcare policy changes.
LinkingPros gave me scholarship to become Certified in Public Health (CPH) through the National Board of Public Health Examiners (NBPHE).
Common pain points
Have you ever thought of the following?
Does your solution have a holistic Proof of Concept?
Potential impacts to current Standard of Care?
Shortfalls of current approved drugs/solutions?
Potential threats from the ongoing trials by competitor?
A clinical data is 1%, 5%, or 20% better than yours?
The possibility for an agency to release a new guidelines?
What difference a high-stake meeting with agency could make?
The amount of fund you would need to bring the product to market?
A gap analysis or pressure test could save you millions?
Same thoughts bothering you? Get in touch
How We Help
We Help you strategize, facilitate & streamline.
From an idea to market approval, LinkingPros helps to Strategize for your product development, to Facilitate your time to market, and to Streamline and guide you through the whole process!
Strategize
Start-up to mid-sized healthcare companies don’t usually have the luxury to hire top-notched expertise they require to strategize for their global development.
LinkingPros offers executive level expertise for your...
Business Development Strategy
Integrated Product Development Strategy
Process Development Strategy
Global Regulatory Strategy
Risk Management Strategy
Facilitate
Healthcare companies in the West and the East usually have different mindset in culture, budget and value. It makes additional layers of barrier to overcome in global development.
LinkingPros offers executive level professionals to meet your...
Strategy planning
Regulatory compliance level
Time-to-market schedule
Talent needs
Budget expectation
Streamline
LinkingPros strives to streamline the global development process to accelerate patient access to medical therapies, across various fields.
Staff from Pharma & Biotech industry
Project teams across multiple time zones
Staff from Regulatory Agencies
Guidance for every phase of drug development
Trusted therapeutic proficiency
Regulatory and Payer Advisory Board
Network of over 1000 experts
Multi-layer Service
We follow state-of-the-art processes to deliver healthcare solutions.
• GxP audits, correction and CAPA management
• Inspection readiness
• Safety process and governance design
• Establishment of QP office (QPPV+)
• Operational process design and procedural implementation
• Quality Management Systems best practice
• Current and prospective market analysis
• Competition landscape analysis
• Development risk and opportunity assessment
• Health authority mapping
• FDA/EMA Advisory Board advice and challenge
• Pipeline review and prioritisation
• Acceleration strategies
• Integrated development plan for approvability and access
• Gap analysis and solutions
• Assessment criteria (in vitro biology, in vitro ADME, pharmacology, PK profile, safety profile etc.) for candidate selection
• Feasibility evaluation for product development
• Translational strategy
• Pilot safety study design
• First-time-in-man considerations
• Interpretation for extension into clinical proof of concept
We also provide consultation services on best strategy for IND planning. Our professionals have extensive experiences in small molecule, biologics, gene therapy, cell therapy and medical devices.
In addition, we can team you up with the best preclinical CROs.
Our professionals would assist with study designs, review the study data and help addressing any potential issues at occurring.
Navigating through the phases of clinical development research is easier with a concise plan. At LinkingPros, we can work together to create your strategy and execute it through our end-to-end solutions.
We can take you through phase I first in human (FIH), phase II a) proof of concept (POC), phase II b) dose confirmation, to phase III registration studies.
We can also support in the preparation and review of the regulatory filing documentation.
Our professionals can also support you in the preparation of the submissions, help prepare you for Agency hearings, and review your submission packages. We can assist to facilitate clear communication with the Agency. We can provide specific support for high-stakes meetings such as FDA Advisory Committee, Oral Explanations, Scientific Advice and HTA advice, Parallel Advice, PRAC public hearings, EMA public workshops, Pricing negotiation preparation and other milestone meetings.
Do you have a particular need or a burning question?
We at LinkingPros will guide you through the maze.
Or, Are you a medical consultant? Join our network.
Let's work together, whenever, wherever.