---
title: Crystal Bio Solutions Scientific Symposium & Reception
description: Join Bay Area biotech and biopharma leaders for the CBS Scientific Symposium & Reception, an afternoon of expert talks and executive networking on bioanalysis, biomarkers, and clinical pharmacology strategies accelerating drug development.
image: https://www.crystalbiosolutions.com/hubfs/e58a70bc-953e-4dbb-9df6-06c3e5ffbd2b-1.png
---

![Logo\_CBS-横版-原色(RGB)](https://www.crystalbiosolutions.com/hs-fs/hubfs/Logo_CBS-%E6%A8%AA%E7%89%88-%E5%8E%9F%E8%89%B2(RGB)-2.png?width=330&height=150&name=Logo_CBS-%E6%A8%AA%E7%89%88-%E5%8E%9F%E8%89%B2(RGB)-2.png)

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Aug 19, 2026

# Crystal Bio Solutions Scientific Symposium & Reception

Join Bay Area biotech and biopharma leaders for the CBS Scientific Symposium & Reception, an afternoon of expert talks and executive networking on bioanalysis, biomarkers, and clinical pharmacology strategies accelerating drug development.

![Crystal Bio Solutions Scientific Symposium & Reception](https://www.crystalbiosolutions.com/hubfs/e58a70bc-953e-4dbb-9df6-06c3e5ffbd2b-1.png)\\

## Event Details

 

The CBS Scientific Symposium & Reception brings together Bay Area biotech and biopharma professionals for a focused scientific exchange on how integrated bioanalysis, biomarkers, immunogenicity, translational science, and clinical pharmacology can support more efficient drug development.

 

**Date:** October 13, 2026

**Time:** 12 PM to 7 PM PDT

**Location:** AC Hotel By Marriott San Francisco Airport Oyster Point/Waterfront,

1333 Veterans Boulevard, South San Francisco, CA 94080

 

Attendance is free of charge for qualified biotech and pharma R&D professionals. This is an open gathering for the San Francisco biotech community.

 

For logistical information, contact:

[cbs\_bd@crystalpharmatech.com](mailto:cbs_bd@crystalpharmatech.com)

 

Event starts in

5days3hrs8min

Don't miss the chance, register now!

 

 

 

## Event Agenda

 

![Meina Liang](https://www.crystalbiosolutions.com/hs-fs/hubfs/Headshots/Untitled%20design%20(7).png?width=140&height=140&name=Untitled%20design%20(7).png)

Meina Liang, Ph.D.

CSO and Head of Bioanalysis & Biomarkers  
**Crystal Bio Solutions**

![Inna Vainshtein](https://www.crystalbiosolutions.com/hs-fs/hubfs/Headshots/Untitled%20design%20(10).png?width=140&height=140&name=Untitled%20design%20(10).png)

Inna Vainshtein, Ph.D.

Senior Director of Bioanalysis & Biomarkers  
**Crystal Bio Solutions**

![Kaia Sartori](https://www.crystalbiosolutions.com/hs-fs/hubfs/Headshots/Kaia.png?width=140&height=140&name=Kaia.png)

Kaia Sartori

Founder and CEO  
**Discovery Bioanalytical Consulting, LLC**

![Jintang He](https://www.crystalbiosolutions.com/hs-fs/hubfs/Headshots/Untitled%20design%20(8).png?width=140&height=140&name=Untitled%20design%20(8).png)

Jintang He, Ph.D.

Senior Principal Scientist  
**Genentech**

![Preeti Paliwal](https://www.crystalbiosolutions.com/hs-fs/hubfs/Headshots/Untitled%20design%20(9).png?width=140&height=140&name=Untitled%20design%20(9).png)

Preeti Paliwal, Ph.D.

Director, Clinical Biomarkers Translational Development  
**Annexon Biosciences**

![Lorin Roskos](https://www.crystalbiosolutions.com/hs-fs/hubfs/Headshots/Untitled%20design%20(5).png?width=140&height=140&name=Untitled%20design%20(5).png)

Lorin Roskos, Ph.D.

CSO and Head of Quantitative Clinical Pharmacology  
**Crystal Bio Solutions**

![Kourosh Parivar](https://www.crystalbiosolutions.com/hs-fs/hubfs/Headshots/Untitled%20design%20(4).png?width=140&height=140&name=Untitled%20design%20(4).png)

Kourosh Parivar, M.Pharm.

Senior VP, Head of Clinical Pharmacology & Pharmacometrics  
**Revolution Medicines**

---

| 12:00–12:30 pm | **Registration & Light Lunch** |
| --- | --- |
| 12:30–12:40 pm | **Welcome & Symposium Introduction**, Meina Liang, Ph.D. |
| 12:40–1:00 pm | **Integrated Bioanalytical Strategies for PK, Biomarker, and Immunogenicity Assessments Across Therapeutic Modalities Supporting Regulatory Approval**, Meina Liang, Ph.D. Pharmacokinetic (PK), biomarker, and immunogenicity assessments are critical to the successful development and regulatory approval of new therapeutics. While regulatory expectations are relatively well established for mature modalities such as small molecules and antibodies, expectations for emerging and novel drug modalities continue to evolve. This presentation will discuss key strategies and considerations for PK, biomarker, and immunogenicity assessments across drug development stages and therapeutic modalities, with a focus on supporting regulatory submissions. Selected case examples will illustrate practical approaches and modality-specific considerations. |
| 1:00–1:20 pm | **Immunogenicity Characterization Tier Analysis for Biotherapeutics: Neutralizing Anti-Drug Antibody and Domain Specificity Assays**, Inna Vainshtein, Ph.D. Immunogenicity assessment is a critical component of biotherapeutic development, as anti-drug antibodies (ADAs) may affect pharmacokinetics (PK), therapeutic efficacy, and patient safety. Regulatory expectations for immunogenicity bioanalytical methods emphasize assay robustness, sensitivity, and drug tolerance to support reliable clinical interpretation. While ADA screening, confirmatory, and titer assays are relatively mature methodologies, characterization assays, including neutralizing antibody (NAb) and domain specificity assays, are often more complex to develop, optimize, and validate. This presentation will discuss the immunogenicity characterization tier, with a focus on regulatory expectations, current challenges, and solutions for NAb and domain specificity assessments. |
| 1:20–1:40 pm | **Navigating Complex Peptide ADA Strategies: What to do When?**, Kaia Sartori Exploring a case example of phase appropriate ADA strategies and assays for a peptide-nanobody construct. This will include ADA strategy for discovery bioanalysis, GLP-Tox, and Clinical Phase 1-3, and will include ADA/NAb examples. |
| 1:40–2:00 pm | **ADC Bioanalysis: Navigating Complex PK and Biotransformation in Drug Development**, Jintang He, Ph.D. This presentation explores bioanalytical strategies for assessing the pharmacokinetics (PK) and biotransformation of antibody-drug conjugates (ADCs), covering conventional assay methodologies, key bioanalytical challenges, and the new opportunities offered by emerging technologies. |
| 2:00–2:20 pm | **Bridging Biology Across Populations: Biomarkers for Global Evidence Generation**, Preeti Paliwal, Ph.D. This presentation explores how biomarker evidence can demonstrate shared disease biology across patient populations, strengthen confidence in cross-regional evidence, and inform global clinical development and regulatory decision-making. |
| 2:20–2:45 pm | **Networking Break** |
| 2:45–3:00 pm | **Challenges and Strategies for Clinical Dose Optimization**, Lorin Roskos, Ph.D. For non-oncology indications, randomized, parallel-group Phase 2 studies with efficacy and pharmacodynamic biomarker endpoints have long been the standard approach for selecting the dosing regimen for Phase 3. These studies typically include a suboptimal dose to characterize the exposure–response relationship. In oncology, the traditional approach of identifying a maximum tolerated dose (MTD) from Phase 1 dose-escalation cohorts can be poorly suited to products whose efficacy exposure–response relationship plateaus below the MTD. FDA's Project Optimus has shifted expectations toward comparison of two or more doses before registrational trials, and dose finding is now often conducted in Phase 1 expansion cohorts. The central challenge in oncology is to evaluate doses that may improve safety without using a suboptimal dose that could worsen survival outcomes. For both oncology and non-oncology indications, biomarker strategies can bracket the low and high ends of the dose range under study. Exposure–response and exposure–safety analyses can then be used to quantitatively predict the optimal dose for registrational trials. These approaches can shorten timelines, reduce cost, and increase the probability of success. |
| 3:00–3:20 pm | **Project Optimus: Opportunities & Challenges**, Kourosh Parivar, M.Pharm. |
| 3:20–3:40 pm | **Poster Session** |
| 3:40–4:10 pm | **Panel Discussion: What Bay Area Biotechs Need from Their Bioanalytical and Clinical Pharmacology Partners**, moderated by Young Neyman |
| 4:10–7:00 pm | **Executive Networking Reception & Happy Hour** |

---

 

---

 

 

## Who This Symposium Is For

 

Clinical Pharmacology Leaders

Dose optimization, PK/PD modeling, and exposure-response analysis.

Bioanalytical Scientists

Assay development, validation, and immunogenicity strategy.

Biomarker Scientists

Translating biomarker data into development decisions.

Translational Medicine Professionals

Bridging nonclinical data to first-in-human strategy.

DMPK Professionals

ADME, PK translation, and modality-specific development.

Clinical Development Leaders

Program strategy across Phase I–III studies.

Clinical Operations Professionals

Trial execution, sample logistics, and site coordination.

Directors, VPs & Senior Scientists

Across biotech and biopharma organizations.

 

 

## Scope of Discussion: Our Expertise

 

Bioanalysis & Biomarkers Expert-driven, GLP-compliant bioanalysis and biomarker solutions built for diverse modalities and innovative pipelines. Quantitative Clinical Pharmacology We provide strategic insight backed by robust data gathering and interpretation, to accelerate decision-making from IND to NDA.

 

These discussions are exploratory. Formal project scoping or regulatory advice requires structured engagement and confidentiality agreements.

 

 

## What You'll Walk Away With

 

 

01

Scientific Insights

Practical approaches to bioanalysis, immunogenicity, ADC assays, dose optimization, and biomarker strategy, grounded in real case studies.

02

Peer-to-Peer Learning

Hear directly from industry leaders and invited speakers, and join a live panel on what Bay Area biotechs need from their partners.

03

Valuable Networking

Connect with scientific leaders, executives, and peers across the Bay Area biotech ecosystem over lunch, breaks, and the reception.

 

 

 

 

## Event Venue

 

![exterior\_sunset\_high\_resolution (1)](https://146565877.fs1.hubspotusercontent-eu1.net/hub/146565877/hubfs/exterior_sunset_high_resolution%20(1).png?width=1200&length=1200&name=exterior_sunset_high_resolution%20(1).png)

![Liberty Pre-Function\_same\_aspect\_fullres](https://146565877.fs1.hubspotusercontent-eu1.net/hub/146565877/hubfs/Liberty%20Pre-Function_same_aspect_fullres.png?width=1200&length=1200&name=Liberty%20Pre-Function_same_aspect_fullres.png)

![Liberty Ballroom\_empty\_same\_aspect\_fullres](https://146565877.fs1.hubspotusercontent-eu1.net/hub/146565877/hubfs/Liberty%20Ballroom_empty_same_aspect_fullres.png?width=1200&length=1200&name=Liberty%20Ballroom_empty_same_aspect_fullres.png)

![Liberty 1 Theatre\_same\_aspect\_fullres](https://146565877.fs1.hubspotusercontent-eu1.net/hub/146565877/hubfs/Liberty%201%20Theatre_same_aspect_fullres.png?width=1200&length=1200&name=Liberty%201%20Theatre_same_aspect_fullres.png)

![Liberty Classroom - Copy\_same\_aspect\_fullres](https://146565877.fs1.hubspotusercontent-eu1.net/hub/146565877/hubfs/Liberty%20Classroom%20-%20Copy_same_aspect_fullres.png?width=1200&length=1200&name=Liberty%20Classroom%20-%20Copy_same_aspect_fullres.png)

![AC Patio2\_same\_aspect\_fullres](https://146565877.fs1.hubspotusercontent-eu1.net/hub/146565877/hubfs/AC%20Patio2_same_aspect_fullres.png?width=1200&length=1200&name=AC%20Patio2_same_aspect_fullres.png)

![Patio\_existing setup\_same\_aspect\_fullres-1](https://146565877.fs1.hubspotusercontent-eu1.net/hub/146565877/hubfs/Patio_existing%20setup_same_aspect_fullres-1.png?width=1200&length=1200&name=Patio_existing%20setup_same_aspect_fullres-1.png)

 

 

## Frequently Asked Questions

 

Is registration required for the symposium?

Yes, please register on this page. Attendance is free for qualified biotech and pharma R&D professionals.

 

Is this a technical seminar or presentation?

Yes. The symposium features scientific presentations on bioanalysis, biomarkers, and clinical pharmacology, along with industry case studies and a panel discussion. The full agenda is above.

 

Who should attend?

Bioanalytical and biomarker scientists, clinical pharmacology and DMPK professionals, translational medicine and clinical development leaders, and senior scientists across biotech and biopharma organizations.

 

Is there a networking component?

Yes. Networking takes place during lunch and breaks, and the day closes with an executive networking reception at the same venue.

 

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