Press Registration Guidelines

To be eligible, applicants must regularly cover the life sciences sector and provide recent bylined articles or reports from the past 180 days.

• Publishers, marketing and PR professionals, sales representatives, and executives without a media role.
• Individuals producing confidential or company-sponsored content.
• Private consultants contracted by a single company (they should request access through their client).
• Representatives of organizations that host competing events may be restricted from access.

• Video and audio recording are not permitted during speaker presentations unless they have given permission to you.
• We may request documentation to verify credentials.
• We reserve the right to deny press passes at our discretion.
• Past press credential holders are not guaranteed future passes

✔️ Accelerate development with optimized CMC strategies

✔️ Master next-gen analytical techniques and QC

✔️ Streamline regulatory pathways to market

✔️ Scale manufacturing with confidence

✔️ Design breakthrough drug-like properties

✔️ Fast-track candidate selection

✔️ Optimize clinical trial design

✔️ Benchmark against industry leaders

✔️ Maximize yield and process efficiency

✔️ Navigate complex regulatory requirements

✔️ Implement cutting-edge QC technologies

✔️ Master emerging molecule challenges

✔️ Engineer superior peptide designs

✔️ Revolutionize delivery systems

✔️ Accelerate discovery pipeline

✔️ Learn from clinical success stories

✔️ Pioneer mRNA design breakthroughs

✔️ Master advanced delivery technologies

✔️ Transform genome editing capabilities

✔️ Scale manufacturing successfully

✔️ Unlock targeted delivery solutions

✔️ Pioneer oral peptide delivery

✔️ Revolutionize device-based strategies

✔️ Optimize macromolecular delivery