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WuXi TIDES · A WuXi AppTec platform

End-to-End CRDMO Platform for Oligonucleotide & Peptide

Discovery, CMC development and the entire manufacturing supply chain for TIDES molecules — under one roof, one quality system, one continuous scale from nanomole to metric tonne.

Scale nmol → mol SPPS reactor volume 100,000 L Sites 10 Scientists 1,600+ Catalogue 3,234 products
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Global Platform, One Vision
Scientists
0Across discovery, development and manufacturing
Sites
0R&D and manufacturing in Asia, Europe and North America
SPPS capacity
0Total solid phase peptide synthesis reactor volume

About Us

One roof for the whole
TIDES supply chain.

WuXi TIDES, a unique Contract Research and Development Manufacturing Organization platform, is an integral part of WuXi AppTec. We offer worldwide partners efficient, flexible and high-quality solutions for the drug development of oligonucleotides, peptides and related synthetic conjugates.

Over 1,600 scientists across 10 R&D and manufacturing sites deliver discovery synthesis, process development and manufacturing of novel monomers, linkers and ligands, oligonucleotides, peptides and complex synthetic conjugates at any scale. Beyond chemistry we offer formulation development, manufacturing, packaging, labeling and distribution in a variety of oral and injectable dosage forms and filling formats.

Our comprehensive analytical method development, validation and testing platform supports TIDES drug development from discovery through clinical to commercial for both drug substance and drug product — and our regulatory dossier teams are experienced in global filings with all major agencies.

Read the full story

The candidate journey

Preclinical to commercial
without changing hands.

An integrated CMC platform means the team that made your first hundred milligrams is still on the file when you validate at tonne scale.

Stage 01

Discovery

High-throughput library and custom synthesis, conjugation, monomer and ligand design with dedicated analytical support.

Stage 02

Preclinical

Route scouting, pre-formulation and tox supply — moving grams to kilograms without changing partners.

Stage 03

Phase I–II

Process development, GMP API, drug product and the CMC package that carries an IND across major agencies.

Stage 04

Phase III

Process validation, scale-up into dedicated suites and stability programmes run under one global quality system.

Stage 05

Commercial

Validated commercial supply across China, Singapore, Switzerland and the United States, with dual-site redundancy.

API

Process R&D, API and intermediates manufacturing at any scale.

Drug Product

Pre-formulation, formulation and process development, oral and injectable manufacturing.

Analytical

Method development and validation, quality control, characterisation and stability.

Regulatory CMC

Dossier preparation supporting global regulatory filings for TIDES molecules.

See the oligonucleotide candidate journey

Why WuXi TIDES

Six reasons programmes
arrive early.

The advantages compound: one quality system, one analytical platform, one set of scientists who already know the molecule.

01

Scalability

From discovery to commercialisation entirely within WuXi TIDES, with readily available large R&D and manufacturing capacity.

02

Conjugation Chemistry

Seamless collaboration across the oligonucleotide, peptide and small molecule teams — the conjugates nobody else wants to touch.

03

New Technology

Biocatalysis for gRNA synthesis, thin film evaporation, reactor-in-series with PAT, continuous flow chromatography, TFF.

04

Global Quality Standard

One quality system across every site, approved by the major regulatory agencies around the world.

05

Comprehensive Analytical

Method development and validation, IPC and release testing, characterisation and stability under one roof.

06

Integrated CMC

API and formulation development, manufacturing, analytical, dossier preparation and clinical supply as a single programme.

Meeting global quality standards

Inspected, repeatedly,
on four continents.

One quality system across every site — and the inspection record to show that it holds wherever your filing lands.

0
US FDA
2013–2025
0
EU EMA
2009–2025
0
China NMPA
2015–2025
0
Japan PMDA
2019–2024
0
South Korea MFDS
2022
0
SwissMedic
2018–2025

What's new

Evidence, not adjectives.

Case studies, inspection outcomes and capacity news from the TIDES platform.

PerspectiveSep 2, 2025

Lower PMI in Peptide Synthesis: Achievable, Measurable, and Scalable

Process mass intensity (PMI) is one of the most important metrics in sustainable manufacturing. It measures the total mass of raw materials required to produce a given mass of product. In…

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Case StudyJul 23, 2025

Case Study: Enable an Innovative GLP-1 GCG Dual Peptide Program IND filing in Just 10 Months

As GLP-1 receptor agonists continue to redefine treatment for metabolic diseases, drug developers are racing to bring new and more complex therapies to the clinic. But innovation alone is…

Read
NewsApr 1, 2025

WuXi AppTec’s Changzhou and Taixing API Sites Successfully Pass FDA Inspections

Shanghai, China – April 1, 2025 — WuXi AppTec, a global company that provides a broad portfolio of R&D and manufacturing services to enable companies in the pharmaceutical and life sciences…

Read
NewsNov 18, 2024

WuXi AppTec’s Couvet Site Receives EcoVadis 2024 Silver Medal Rating

Couvet, Switzerland – November 14, 2024 – WuXi AppTec, a global company that provides a broad portfolio of R&D and manufacturing services to enable companies in the pharmaceutical and life…

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All news Resource library Events

How can we help?

Our TIDES drug experts stand ready.

Tell us where your molecule is today — discovery, CMC, or commercial supply — and we will map the fastest credible route to patients.

Small molecule projects? WuXi STA