Pharmaceutical Microbiology East CoastConference & Workshops • Boston, USA
Science • Regulation • Sterility Assurance

Pharmaceutical Microbiology East Coast

A specialist meeting for pharmaceutical microbiologists, contamination control experts, quality leaders, and regulators to share practical strategies for safer sterile manufacturing.

28–29 OctoberTwo-day conference
30 OctoberInteractive workshops
Boston, MAUnited States
3rd AnnualIndustry-led technical conference
25+Expert speakers
16Technical sessions
2Specialist workshops
1Focused community

Build resilient microbial control strategies with the people shaping the field.

The programme explores contamination control, rapid microbial methods, endotoxin testing, mycoplasma control, container closure integrity, sterility assurance, and the evolving regulatory landscape.

01 / REGULATION

Translate new expectations into practical action

Discuss Annex 1, USP perspectives, risk assessment, and current inspection priorities with experienced practitioners.

Explore sessions →
02 / TECHNOLOGY

Evaluate emerging microbiology methods

Compare rapid methods, recombinant reagents, automation, and modern testing approaches through real case studies.

View workshops →
03 / COMMUNITY

Learn from cross-functional industry leaders

Connect quality control, manufacturing, regulatory, and R&D perspectives in one focused environment.

Meet speakers →

Two days of applied microbiology.

A concise programme structure inspired by the original East Coast conference focus.

08:30
Registration

Delegate arrival, coffee, and networking

Connect with speakers, sponsors, and fellow pharmaceutical microbiology professionals.

09:15
Opening keynote

Designing a sustainable contamination control strategy

Aligning facilities, people, process, monitoring, and data into an integrated programme.

10:30
Regulatory insight

Container closure integrity and sterility assurance

Risk-based control strategies and practical implications for sterile products.

13:30
Technology spotlight

Rapid microbial methods: implementation lessons

Validation, stakeholder adoption, data integrity, and operational scale-up.

15:45
Panel discussion

Mycoplasma testing: past, current, and future state

Industry perspectives on speed, sensitivity, and regulatory acceptance.

Voices from quality, manufacturing, and science.

Representative speaker cards for the reconstructed conference homepage.

Dr. Elena Morris

Director, Global Microbiology

STERILITY ASSURANCE

Marcus Reed

QC Microbiology Lead

CONTAMINATION CONTROL

Dr. Priya Shah

Principal Scientist

RAPID METHODS

Thomas Keller

Regulatory Strategy Advisor

QUALITY SYSTEMS

Go deeper with interactive technical sessions.

Workshop A

Recombinant chromogenic assays as alternatives for the bacterial endotoxins test

Explore scientific principles, validation expectations, regulatory status, and implementation pathways for synthetic reagents.

Request Details
Workshop B

Modern mycoplasma testing: faster, flexible, and fit for purpose

Review method selection, sampling, controls, investigation readiness, and practical adoption in regulated environments.

Request Details

Created for specialists across the pharmaceutical lifecycle.

Quality control • Sterile manufacturing • Biologics • Cell therapy • Regulatory affairs • Validation • Laboratory technology

Join the microbiology conversation.

Request the programme, workshop information, or future event updates.

Register Interest →