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Capabilities

From a single spot purchase to a full delivery chain

All three partnership models share the same capability backbone: a governed supply network down to the base. The only difference is whether you already own the process. You can start with the smallest step — no need to bet on the entire chain up front.

Three partnership tiers, deepening step by step

Trust is staged: validate delivery discipline with the smallest order first, then move on to program development and tech transfer.

TradeSpot Supply

Best for: Have a defined CAS / spec / quantity

  • Qualified-supplier screening & commercial terms
  • Quality agreements & dossier documents
  • Export, customs clearance & temperature-controlled delivery
  • Dual-use items / ECCN pre-screening
Typical lead time Spot: 2–6 weeks
Generic pharma with registered filings, CDMO procurement
ProgramProgram Development

Best for: Have a target molecule but lack a stable process or compliant capacity

  • Route design & impurity attribution
  • Pilot scale-up & process validation
  • Analytical method development & transfer
  • DMF / CEP document preparation
Typical lead time 3–12 months
Formulators in the filing stage, buyers needing backup supply
Tech TransferTech Transfer

Best for: Need to land the process in your own capacity or a new region

  • Full process package & analytical package transfer
  • On-site scale-up support & validation batches
  • Marketing authorization holder & license arrangements
  • Long-term technical maintenance & iteration
Typical lead time 6–18 months
Localization build-out in emerging markets, MAH holders, regional licensing partners

Three capability layers form a non-replicable delivery discipline

Intelligence decides what to do, the supply network decides whether it can be done, and quality governance decides whether it can be done stably over the long term.

01
Variant Intelligence

Working backward from blockbuster drugs and patent-expiry windows to the demand for key intermediates — we first say what to build, then talk supply. Every candidate runs a four-dimension screen (qualification × capacity × market × compliance) before entering the catalog.

LOE-drivenFour-dimension screeningDemand-side first
View LOE opportunities →
02
Supply Network Governance

Not a matchmaking directory, but a governed capacity network: specialty plants in chiral, fluorination, multi-step coupling, continuous-flow, etc. are classified and on record, each with an audit history, historical batches and a backup plan.

Specialty processes on recordAudit & backupSingle window
View intermediates in stock →
03
Quality Governance

Quality agreements, change control, deviations & CAPA, full-batch COA traceability, plus PCF carbon-footprint data — this is where the coordinator's true technical assets lie.

Quality agreementDeviation & CAPACOA traceabilityPCF
View the delivery platform →

Five coordination functions, one responsible entity

All five coordination functions are held by a single entity that plans and is accountable for the outcome — instead of you having to stitch five suppliers together.

01
Supplier Network

Supplier screening & commercial terms: screened by qualification, capacity, export history and compliance record; commercial conditions folded into the master contract.

02
Audit & Qualification

On-site audit & CAPA closure: audit findings and corrective actions are closed within the project — problems are not thrown back to the buyer.

03
Logistics & Trade

Export, customs clearance & delivery: including dual-use items / ECCN pre-screening, cold chain and temperature-control documentation.

04
Process & Technical

Route, impurity & scale-up: synthetic route evaluation, impurity attribution, scale-up and process validation.

05
Regulatory Advisory

DMF, CEP & filing documents: prepare CTD modules by target country and maintain across the lifecycle.

Single Responsible Entity

Unibest — one contract, one plan, one escalation window.

Chemistry capability on call

Process capabilities callable by route choice

The following are stable capacities owned by group entities or already brought under governance agreements, matched to molecular difficulty — not sourced ad hoc from whoever is cheapest.

Chiral synthesis & resolution

Asymmetric synthesis, enzymatic and crystallographic resolution are evaluated in parallel, compressing step count while preserving enantiomeric purity — suited to single-isomer intermediates.

Fluorination chemistry

Fluorination, trifluoromethylation and fluorinated building-block construction, covering both selective fluorination and late-stage introduction strategies.

Multi-step cross-coupling

Scale-up condition development for Suzuki, Buchwald–Hartwig, Negishi and other couplings, including catalyst selection and metal-residue control.

Heterocycle construction

Multi-route comparison for heterocyclic systems such as pyridine, pyrimidine, indole and triazole, used for patent avoidance and cost optimization.

Continuous-flow & microreactor engineering

Built on Zhejiang Tize Pharmaceuticals' continuous-flow technology platform, rapid condition screening is converted into directly scalable continuous processes, improving safety and yield stability.

AI-assisted route design

AI drug-design and process-prediction capabilities on the same platform, used for candidate-route ranking, impurity-risk prediction and scale-up condition recommendations.

Green chemistry & LTS cryogenic supercritical

Built on Guangzhou Taqing Environmental's Low-Temperature Supercritical (LTS) green technology, reducing waste and energy use while improving separation and purification efficiency.

LNP & complex injectables

Built on Shanghai Daoyi Zhenhe Biotechnology's lipid nanoparticle delivery capability, covering lipid formulation, encapsulation and lyophilization process development.

Continuous-flow process platform

Intrinsically safer continuous process development

Moving batch parameters onto continuous equipment unchanged is the most common way this route fails. The capabilities below are supported by Zhejiang Tize Pharmaceuticals; each is assessed per molecule and route before scheduling.

The industry pain point

The biggest obstacle in shifting from batch vessels to continuous flow is thatbatch process parameters do not transfer to continuous processes. Hand the design to a team that builds equipment but knows neither organic chemistry nor reaction engineering, and production stays inefficient indefinitely.

How Tize approaches it

Kinetic models plus AI surrogate models are used to design and optimize the reaction parameters of each continuous process, rather than moving batch parameters straight onto continuous equipment.

Four core technologies

A closed loop from safety boundary to parameter control to intelligent optimization
01
Continuous flow raises intrinsic safety

A very high surface-to-volume ratio and excellent heat removal keep in-line hazardous inventory and potential temperature rise low; the inherent flame resistance and explosion protection of piping turn formerly runaway-prone reactions into intrinsically safe processes.

02
Kinetic models pin down reaction conditions

Reaction-path analysis and AI fitting of experimental data build the kinetic model that governs selectivity; the influence of temperature and molar flow ratio on selectivity is simulated to derive high-selectivity parameters and tailor the process to specific continuous equipment.

03
Bayesian optimization for process design

For unclear mechanisms, multiphase catalysis and multi-objective multi-unit operations, AI surrogate statistical models led by Bayesian optimization complement the kinetic model — approaching the global optimum without fitting the function as a whole and returning a Pareto front.

04
In-line analysis upgrade

In-line techniques such as ReactIR and Spinsolve NMR, combined with artificial neural networks, estimate reaction-component concentrations in real time for multi-step monitoring and push process optimization toward full automation.

Batch vessel vs continuous flow: intrinsic safety

Redesigning the process boundary of hazardous reactions around intrinsic safety
AspectBatch vesselContinuous flow
Reaction volumeLarge volume required, poor coolingHigh surface-to-volume ratio, excellent heat removal
Hazardous inventoryHigh reactant concentration, large in-line inventoryHigh at the inlet, decreasing along the path, small in-line inventory
Reaction controlOnly through reactor temperatureExcellent heat removal plus heat-dilution effect
Cooling failureEmergency handling requiredInherent flame resistance of piping, strong explosion protection

Measured gains in continuous synthesis

Continuous synthesis · Diazo reaction
1000–4000×
Smaller liquid holdup, substantially improving intrinsic safety
80%↓
Lower energy consumption
30%↓
Lower wastewater discharge, sharply fewer by-products
Continuous synthesis · Nitration
3 levels↓
Lower reaction-risk assessment level
hours → minutes
Reaction time cut by orders of magnitude
10%↑
Higher yield, more consistent quality

Reaction types with continuous capability

Hazardous and strongly exothermic reactions suited to continuous conversion
Diazotization and its derivativesNitrationOxidationHydrogenationCyclizationHigh-viscosity reactionsAminationSelective mono-acylation (etherification)

The figures above are measured values from existing projects under specific molecules and process conditions; they are not a commitment for any particular project. Suitability for continuous operation and the achievable gain must be assessed case by case.

Project delivery chain

Route design → scale-up → commercial supply · handled by the group's own CDMO bases

No change of contact across the chain: process, quality, regulatory and supply are advanced through a single project window.

Custom Synthesis

Around the target molecule and project stage, we provide route assessment, compound preparation and technical coordination — for compounds not in the catalog.

Route assessmentmg–kg scaleProject-custom
Development & Scale-Up

As the project evolves, we engage process R&D, analytical methods and scale-up production resources until commercial readiness.

Process R&DAnalytical devPilot scale-up
QC & Regulatory Dossier

Quality control, impurity profile and regulatory documentation are advanced together; modules required for DMF / CEP are prepared by target market.

Process validationImpurity studyDMF / CEP
Supply Continuity

Continuous supply is secured through batch scheduling and backup capacity, reducing the stock-out risk of a single site and a single batch.

Commercial supplyBackup capacityLifecycle
Tech Transfer

Complete transfer of process, analytical methods and documents between pilot and commercial bases, shortening the scale-up cycle.

Process transferMethod transferScale-up verification
Project Coordination

A single project window connects the demand side with the group's R&D, manufacturing and research resources, reducing multi-party coordination.

Single point of contactCross-site coordinationCross-timezone

Group growth path

Four phases

From chemical trading in Ningbo in 2003 to a group network spanning R&D, CDMO, formulations, green technology and global market platforms.

2003 – 2007
From trading to in-house R&D

Chemical trading built the first customer and supply-chain base; the group then moved into pharma intermediates and new-material R&D.

  1. 2003Ningbo Unibest · Global HQ
    Group headquarters
    China · Ningbo
  2. 2007Shanghai Unibest Biopharma
    Pharma intermediates & new materials R&D
    China · Shanghai
2008 – 2010
Building manufacturing and the value chain

CDMO capacity for chemical drugs and APIs connected R&D output to production.

  1. 2008Xi'an Caijing
    CDMO for chemical drugs & intermediates
    China · Xi'an
  2. 2010Jiangsu Weikaier
    CDMO for APIs & pharma intermediates
    China · Nanjing
2018 – 2022
Formulations, green tech, capital and technology platforms

Adding four capabilities: formulation MAH, green processes, industrial investment and AI-driven process development.

  1. 2018Shenzhen Aoqi Biopharma
    Formulation MAH
    China · Shenzhen
  2. 2018Guangzhou Taqing Environmental
    LTS green environmental technology
    China · Guangzhou
  3. 2020Ningbo Qiandexinlong
    Industrial investment & holding platform
    China · Ningbo
  4. 2022Zhejiang Tize Pharmaceuticals
    AI drug design · continuous flow · mechanochemistry
    China · Hangzhou
2023 – 2026
Global network and new modalities

Overseas business platforms established one after another, and entry into macromolecule LNP delivery systems.

  1. 2023Asia-Pacific business center
    New Zealand · Auckland
  2. 2024European market access
    France · Paris
  3. 2024North American commercial resources
    USA · New York
  4. 2025SingaPharma Pte. Ltd.
    Pharma import & regional licensing
    Singapore
  5. 2026Shanghai Daoyi Zhenhe Biotechnology
    Macromolecule LNP delivery systems
    China · Shanghai
2003
Founded
50+
Countries covered
16
NDA / BLA filings
100+
IND filings

How the capabilities empower each other

The group is not a flat collection of companies but a top-down empowerment chain: capital and governance provide the foundation, technology and process deliver scalable solutions, manufacturing and compliance carry out scale-up and registration, global platforms land products and rights in specific markets — and market requirements flow back into R&D.

FoundationCapital & governance platform

Industrial investment, holding and team incentives provide long-term capital and a governance framework for the operating entities.

Ningbo Unibest · Global HQ
Group headquarters
China · Ningbo · 2003
Ningbo Qiandexinlong
Industrial investment & holding platform
China · Ningbo · 2020

Capital empowerment·A single investment platform invests externally while operating entities focus on their own business.

TechnologyTechnology & process R&D platform

Pharma intermediates and new-material R&D, combined with AI drug design, continuous flow and mechanochemistry, delivers scalable routes and reaction conditions.

Shanghai Unibest Biopharma
Pharma intermediates & new materials R&D
China · Shanghai · 2007
Zhejiang Tize Pharmaceuticals
AI drug design · continuous flow · mechanochemistry
China · Hangzhou · 2022

Process & route empowerment·Tize's technology platform recommends candidate routes and reaction conditions to the CDMOs, reducing scale-up risk.

ManufacturingManufacturing & compliance platform

CDMO for chemical drugs and intermediates, API CDMO, formulation MAH and macromolecule LNP delivery — carrying scale-up and registration files.

Xi'an Caijing
CDMO for chemical drugs & intermediates
China · Xi'an · 2008
Jiangsu Weikaier
CDMO for APIs & pharma intermediates
China · Nanjing · 2010
Shenzhen Aoqi Biopharma
Formulation MAH
China · Shenzhen · 2018
Shanghai Daoyi Zhenhe Biotechnology
Macromolecule LNP delivery systems
China · Shanghai · 2026

Product & rights empowerment·Products and registration files from the manufacturing layer are landed by the global platforms.

MarketGlobal market platform

Regional entities handle import, licensing, registration and commercialisation, landing products and rights in specific markets.

Cross-border settlement & licensing platform
Hong Kong, China
SingaPharma Pte. Ltd.
Pharma import & regional licensing
Singapore · 2025
Asia-Pacific business center
New Zealand · Auckland · 2023
European market access
France · Paris · 2024
North American commercial resources
USA · New York · 2024

Market & regulatory feedback·Registration and quality requirements of target markets define the next steps for R&D and processes.

Cross-cuttingGreen manufacturing plugged directly into production

Guangzhou Taqing Environmental (LTS low-temperature supercritical technology, 2018) provides green process and waste-reduction solutions to every manufacturing base. It reaches into both the technology and the manufacturing layer rather than forming a layer of its own.

Entities and years are compiled from public disclosures; entries within a phase are ordered by year of entry. Shareholding ratios and intra-group transaction arrangements are not public information.

Scope 3-Ready Supply

Low-Carbon Intermediates for EU and US buyers
Qualified Material

Spec-driven intermediates, held to the same qualification discipline as every Unibest project.

Auditable PCF Data

Product carbon-footprint data packaged to the buyer's Scope 3 disclosure requirements.

Reduction Plan

A continuous decarbonization roadmap maintained with the production site — not a one-off static figure.

Compliance Evidence

Methodology notes and evidence chains aligned to common buyer questionnaires.