PharPoint Research to Attend World Vaccine Congress Washington 2021

PharPoint Research will be in virtual attendance at the event, which is being held from May 4th to May 6th.

 

About the World Vaccine Congress

The conference, organized by Terrapinn, is the “largest, most established meeting dedicated to vaccines.” Attendance at the event is free. To sign up, visit the Terrapinn website.

This year, the event is expected to cover:

  • COVID-19
  • Immune Profiling
  • Cancer Immunotherapy
  • Respiratory & Infectious Disease
  • Vaccine Safety
  • Clinical Dvelopment
  • Market Access
  • Vaccine Supply & Logistics
  • Bioprocessing & Manufacturing
  • Biodefence
  • Anit-Microbial Resistance
  • One Health

 

Keynote speakers attending the event include the WHO’s Director of Vaccines Dr. Kate O’Brien, the COO of COVAXX Christina Yi, and the CMO of Moderna Dr. Tal Zaks, among many others. PharPoint’s team is thrilled to be in attendance, and looking forward to hearing from and speaking with attendees.

About PharPoint Research

As an award-winning CRO, the PharPoint Research team has extensive experience within infectious disease, including 5 regulatory submissions and over 300+ studies supported by our biometric team since 2007. PharPoint provides clinical operations, project management, biostatistics, statistical programming, data management, and strategic clinical trial consulting services to clients of all sizes with a 95% client retention rate.

Attending the event and interested in speaking with a member of our team to learn more about how PharPoint’s industry-best standard timelines and infectious disease expertise can support your upcoming study?

Fill out the form below and a representative will be in touch to schedule a time to speak with you.

Are you at a biotech or pharmaceutical company that will be attending this years World Vaccine Congress Washington 2021?

Reserve a spot on our team’s calendars with the form below. We’re looking forward to speaking with you!



RELATED RESOURCES

EBOOK

Standard Clinical Trial Timelines: A Sponsor’s Guide to Evaluating Biometrics CROs

This brief guide provides timeline benchmarks for Sponsors evaluating biometrics contract research organizations (CROs).


Exploring Standard CRO Timeline Benchmarks

Preparing to work with a top biometrics contract research organization and wondering how their promised data management, biostatistics, and medical writing timelines match up to the industry average? To help sponsors dig into these details and ensure the timelines they’re receiving are competitive, we’re providing PharPoint’s typical timelines alongside research that calculates industry standard timelines, when available.

Our hope is that this document can help sponsors set realistic expectations, confidently ask the right questions of their vendors, and ultimately, partner with a top biometrics CRO that keeps their study moving: because patients are waiting.

 

eBook contents include:

PharPoint’s short eBook, Standard Clinical Trial Timelines: A Sponsor’s Guide to Evaluating Biometrics CROs, includes the below information.

  • Standard database build timeline
    • The bigger picture: Considering site identification and study start-up
  • Standard mid-study database change timeline
  • Standard database lock time
    • Six strategies for a faster database lock
  • Evaluating database lock to top line results timeline
    • Ensuring a rapid delivery
  • Evaluating database lock to delivery of tables, listings, and figures (TLF) timeline
  • Standard clinical study report delivery timeline
  • About PharPoint Research

Compare Standard Clinical Trial Timelines

For instant access to the eBook, fill out the form below.


RELATED RESOURCES

EBOOK

Standard Clinical Trial Timelines: A Sponsor’s Guide to Evaluating Biometrics CROs

This brief guide provides timeline benchmarks for Sponsors evaluating biometrics contract research organizations (CROs).


Exploring Standard CRO Timeline Benchmarks

Preparing to work with a top biometrics contract research organization and wondering how their promised data management, biostatistics, and medical writing timelines match up to the industry average? To help sponsors dig into these details and ensure the timelines they’re receiving are competitive, we’re providing PharPoint’s typical timelines alongside research that calculates industry standard timelines, when available.

Our hope is that this document can help sponsors set realistic expectations, confidently ask the right questions of their vendors, and ultimately, partner with a top biometrics CRO that keeps their study moving: because patients are waiting.

 

eBook contents include:

PharPoint’s short eBook, Standard Clinical Trial Timelines: A Sponsor’s Guide to Evaluating Biometrics CROs, includes the below information.

  • Standard database build timeline
    • The bigger picture: Considering site identification and study start-up
  • Standard mid-study database change timeline
  • Standard database lock time
    • Six strategies for a faster database lock
  • Evaluating database lock to top line results timeline
    • Ensuring a rapid delivery
  • Evaluating database lock to delivery of tables, listings, and figures (TLF) timeline
  • Standard clinical study report delivery timeline
  • About PharPoint Research

Compare Standard Clinical Trial Timelines

For instant access to the eBook, fill out the form below.


RELATED RESOURCES