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Pharmalink Consulting A Brief Overview
Who we are ,[object Object],[object Object],[object Object],[object Object],[object Object]
What we can help with ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Who we work with ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Global Experience ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
How we work ,[object Object],[object Object],[object Object],[object Object],[object Object]
How we work ,[object Object],[object Object],[object Object]
Pharmalink Consulting Case Studies
CLIENT:  A major pharmaceutical company based in Europe PROJECT:  A large product compliance project  OBJECTIVE:  Review all European-registered licenses and bring into  compliance with current manufacturing site practices SOLUTION:  Pharmalink provided a dedicated team of regulatory affairs  specialists to work on the project for 3 years One of the key advantages that Pharmalink was able to bring to the project was the ability to adjust the number of consultants working on  the project to fit the client’s needs and hit every deadline whilst always maintaining the level of quality CASE STUDY 1: Major regulatory compliance project
[object Object],[object Object],[object Object],[object Object],[object Object],CASE STUDY 1: Major regulatory compliance project
CLIENT:  Major pharmaceutical company based in Europe PROJECT:  Review and update of a Module 3 and Quality Overall  Summary for a Biosimilar product in preparation for one of the  first European submissions of its type OBJECTIVE:  Document submission.  Speed to market was of high priority to the client SOLUTION:  Pharmalink  was able to turn to one of its experienced  consultants with a track record specifically with the biotech  product in question Accurate review and submission preparation of the QOS and Module 3  The client could utilize the consultant's advice and make submissions according to the planned timeline CASE STUDY 2: Biosimilar product review
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],CASE STUDY 2: Biosimilar product review
CASE STUDY 3: Multinational clinical trial sponsor & Clinical Research Organization CLIENT:  Sponsor and CRO PROJECT:  Provide regulatory support for a clinical trial including new  submissions for the trial in multiple markets OBJECTIVE:  Submit the clinical trial in multiple locations in a timely manner  to allow trial initiation SOLUTION:  Pharmalink provided consultants with valuable local  knowledge to add to the regulatory intelligence of submissions  in each market This project was a testament to the lengths to which the team went to understand the brief and work with the client to achieve their goals
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],CASE STUDY 3: Multinational clinical trial sponsor & Clinical Research Organization
CASE STUDY 4: Multinational clinical trial sponsor & Clinical Research Organization ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],CASE STUDY 4: Product Compliance Project (External) Large Scale Pharmaceutical Company ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
CASE STUDY 4: Multinational clinical trial sponsor & Clinical Research Organization ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],CASE STUDY 4: Product Compliance Project (External) Large Scale Pharmaceutical Company PROJECT DETAILS: Dossiers Collected 270 Dossiers Collated 270 Compliance Assessments Performed 270 (10% TPM) Remediation Packages Prepared 564 Markets AT, BE, BU, CH, CY, CZ, DE, DK, EE, EL,ES, FI, FR, HU, IE, IS,  IT, LT, LU, LV, MT, NL, NO,  PL, PO, RO, SE, SK, UK
CASE STUDY 4: Multinational clinical trial sponsor & Clinical Research Organization ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],CASE STUDY 4: Product Compliance Project (External) Large Scale Pharmaceutical Company ,[object Object],[object Object],[object Object],[object Object],[object Object]
CASE STUDY 4: Multinational clinical trial sponsor & Clinical Research Organization ,[object Object],[object Object],[object Object],[object Object],[object Object],CASE STUDY 5:  Multiple Abridged License Applications Virtual Pharmaceutical Company
CASE STUDY 4: Multinational clinical trial sponsor & Clinical Research Organization CASE STUDY 5: Multiple Abridged License Application Virtual Pharmaceutical Company ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Pharmalink Consulting Additional Information
What else can we offer you? ,[object Object],[object Object],[object Object]
Fees & Pricing ,[object Object],[object Object],[object Object],[object Object]
What Clients say "The project was managed very efficiently by their office-based and on-site staff who are always quick to respond to our needs. We continue to use Pharmalink as our preferred source of consultants for long-term and short-term projects." Large Biotech Company "Many thanks to the Pharmalink project team for doing such a fantastic job. Our MA submissions were delivered very smoothly with impeccable timing." Virtual Pharmaceutical Company   "Each of their staff members have been extremely helpful, efficient, and friendly and have always been willing to go the extra mile to meet our needs." Small Generics Company  "...all projects have been delivered ahead of time or on time. Their experienced and professional approach is mirrored by the resource they supply." Large Generics Manufacturer
[object Object],[object Object],Pharmalink Consulting Our offering in summary
[object Object],[object Object],Pharmalink Consulting Our offering in summary
Thank you ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]

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Learn More About Pharmalink

  • 1. Pharmalink Consulting A Brief Overview
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  • 9. CLIENT: A major pharmaceutical company based in Europe PROJECT: A large product compliance project OBJECTIVE: Review all European-registered licenses and bring into compliance with current manufacturing site practices SOLUTION: Pharmalink provided a dedicated team of regulatory affairs specialists to work on the project for 3 years One of the key advantages that Pharmalink was able to bring to the project was the ability to adjust the number of consultants working on the project to fit the client’s needs and hit every deadline whilst always maintaining the level of quality CASE STUDY 1: Major regulatory compliance project
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  • 11. CLIENT: Major pharmaceutical company based in Europe PROJECT: Review and update of a Module 3 and Quality Overall Summary for a Biosimilar product in preparation for one of the first European submissions of its type OBJECTIVE: Document submission. Speed to market was of high priority to the client SOLUTION: Pharmalink was able to turn to one of its experienced consultants with a track record specifically with the biotech product in question Accurate review and submission preparation of the QOS and Module 3 The client could utilize the consultant's advice and make submissions according to the planned timeline CASE STUDY 2: Biosimilar product review
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  • 13. CASE STUDY 3: Multinational clinical trial sponsor & Clinical Research Organization CLIENT: Sponsor and CRO PROJECT: Provide regulatory support for a clinical trial including new submissions for the trial in multiple markets OBJECTIVE: Submit the clinical trial in multiple locations in a timely manner to allow trial initiation SOLUTION: Pharmalink provided consultants with valuable local knowledge to add to the regulatory intelligence of submissions in each market This project was a testament to the lengths to which the team went to understand the brief and work with the client to achieve their goals
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  • 23. What Clients say "The project was managed very efficiently by their office-based and on-site staff who are always quick to respond to our needs. We continue to use Pharmalink as our preferred source of consultants for long-term and short-term projects." Large Biotech Company "Many thanks to the Pharmalink project team for doing such a fantastic job. Our MA submissions were delivered very smoothly with impeccable timing." Virtual Pharmaceutical Company "Each of their staff members have been extremely helpful, efficient, and friendly and have always been willing to go the extra mile to meet our needs." Small Generics Company "...all projects have been delivered ahead of time or on time. Their experienced and professional approach is mirrored by the resource they supply." Large Generics Manufacturer
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