>
  1. Libraries
  2. AMRI Synthetic Compound Collection (ASCC)
  3. Custom Chemical Library Synthesis
  4. Lead Optimization
  5. CADD
  6. Fermentation
  7. Biocatalysis and Bioprocessing
  8. Catalog Compounds
  9. Insourcing
  10. Drug Development Solutions
  11. Chemical Process R&D
  12. Continuous Flow Processing
  13. Custom Synthesis
  14. Process Safety Assessment
  15. Scale-up Capabilities
  16. High-Potency APIs (HPAPIs)
  17. Preformulation and Material Science
  18. Physical Characterization
  19. Solid Form Screening and Selection
  20. Enantiomeric Resolution
  21. API Process Integration
  22. Bulk Characterization
  23. Formulation Development
  24. Separations Sciences
  25. Chiral Method Development
  26. Chiral Resolution
  27. Chemical Purification
  28. Impurity Isolation and Identification
  29. Bioanalytical Services
  30. Fine Chemicals
  31. Fine Chemicals Catalog
  32. Vinylphosphonic Acid – VPA
  33. Kilo Lab and Small-Scale Manufacturing
  34. Chemical Development
  35. Technologies and Capabilities
  36. Fermentation, Biocatalysis and Bioprocesses
  37. Organometallic Chemistry
  38. Propanephosphonic Acid Anhydride – T3P®
  39. Vinylphosphonic Acid (VPA)
  40. Analytical Services
  41. Analytical Method Development and Validation
  42. Analytical Testing Services
  43. Sample Submission and Forms
  44. Biopharmaceutical Analysis
  45. Chromatography
  46. Diffraction Studies
  47. Gas Testing
  48. Heavy Metals Testing
  49. Biochemistry Services
  50. Regulatory Aspects of Biological Pharmaceuticals
  51. Biochemical and Biosimilar Characterization
  52. Product-Related Impurity Characterization
  53. Aggregation State Characterization
  54. Structure Elucidation
  55. Protein Formulation Development
  56. Comparability Studies
  57. Protein and Peptide Crystallization
  58. Initial Drug Substance Characterization
  59. Mass Spectrometry
  60. Material Testing
  61. Microbiology
  62. Micromeritics
  63. Microscopy
  64. Personal Care Chemistry
  65. Residual Solvents
  66. Sorption and Desorption
  67. Spectroscopy
  68. Structural Characterization
  69. Thermal Analysis and Calorimetry
  70. Water Analysis
  71. Glass Delamination – USP 1660
  72. Unknown Particulate Identification
  73. Particle Characterization
  74. Batch Release and Stability Lot Testing
  75. Method Development and Validation
  76. Solid-State Chemistry and Particle Engineering
  77. Solid Form Screening and Selection
  78. Crystallization Process Development
  79. Computational Methods
  80. PAT and Pharmaceutical Quality by Design
  81. Drug Product and Delivery
  82. Stability, Solubility, Dissolution
  83. Mapping and Imaging Studies
  84. Formulation Services
  85. In Vitro Bioequivalence Testing
  86. Extractables and Leachables
  87. Chemical Characterization
  88. E&L for Pharma and Biotech
  89. Impurities
  90. Toxicological Risk Assessment (TRA)
  91. Container Closure Integrity
  92. Vacuum Decay Leak Detection
  93. Electrical Conductivity (HVLD)
  94. Helium Leak Detection (HeLD)
  95. Residual Seal Force (RSF)
  96. Mass Flow Leak Detection
  97. Laser-Based Headspace Analysis
  98. Airborne Ultrasound / Seal-Scan
  99. Container Qualification
  100. Pharmaceutical Glass
  101. <USP 661> Plastic Containers
  102. <USP 670> Auxiliary Packaging Components
  103. <USP 671> Container Performance
  104. EP & JP Container Testing
  105. Elastomeric Closures
  106. Biological Reactivity
  107. Container Qualification Full Test List
  108. Packaging and Distribution Testing
  109. ASTM & ISTA Distribution
  110. Environmental Conditioning, Cycling and Simulation Testing
  111. Pharmaceutical Package Testing
  112. Medical Device Packaging Testing
  113. Consumer Product Packaging
  114. Shelf Life and Accelerated Aging Testing
  115. Packaging Materials Testing
  116. Package Labeling
  117. Package Strength
  118. Package Integrity
  119. Retains and Complaint Resolution
  120. Environmental Conditioning
  121. ISTA 6 Amazon Testing
  122. Medical Device Testing
  123. Cleaning Validations
  124. ISO 10993 Biocompatibility
  125. ISO 11607 Medical Device Validation
  126. Mechanical and Functional Device Testing
  127. Leak Detection
  128. Dose Delivery
  129. Syringes
  130. Drug Delivery Device Testing
  131. Functional, Mechanical, & Metrology Testing
  132. Small Bore Connector Testing
  133. Complaint Handling
  134. Microbiological Laboratory
  135. Microbial Limits Testing
  136. Bacterial Endotoxin Testing: USP <85>
  137. Antimicrobial Effectiveness – AET
  138. Microbiological Population Verification
  139. USP <87> Biological Reactivity Tests – In Vitro
  140. Disinfectant Efficacy
  141. Environmental Monitoring
  142. Water Testing
  143. Problem Solving
  144. Patent Prosecution and Litigation Support
  145. Intellectual Property Support
  146. Regulatory Support
  147. Counterfeit Analysis
  148. API Development and Manufacturing Solutions
  149. APIs and Intermediates
  150. Custom Synthesis and Contract Manufacturing
  151. Fine Chemicals
  152. Technologies and Capabilities
  153. Fermentation, Biocatalysis and Bioprocesses
  154. Boronic Acids, Biaryls, Grignards and Organolithiums
  155. Sterile APIs
  156. DEA-Controlled Compounds
  157. High-Potency APIs
  158. Halogenations and Other Hazardous Chemistries
  159. Propanephosphonic Acid Anhydride – T3P®
  160. Regulatory Support and QA
  161. Drug Product Solutions
  162. Drug Product Development Capabilities
  163. Drug Product Manufacturing
  164. Vials
  165. Syringes
  166. Bottles
  167. Lyophilization
  168. Sterile University
  169. Stability and Release Testing
  170. Government Contracting
  171. CAS and other designations
  172. Prime Contracts
  173. Subcontracts
  174. News
  175. Events
  176. AMRI Express
  177. In Vitro DMPK
  178. Antimicrobial Discovery
  179. Let’s Get Started
  180. slide icon

    亚博手机客户端|网页版

    Presented by Brian P. Haney, Ph.D., Director of Technical Operations, AMRI
    2020-02-22 | 11:00am EST

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    Antimicrobial Discovery

    AMRI Express Portal

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    We’ve Got Fine Chemicals Down to an Exact Science

    Every Stage, Every Scale – Worldwide

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    We’ve got API Development and Manufacturing Down to an Exact Science

    Access More than 240 Commercial APIs

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    We’ve got Drug Product Down to an Exact Science

    Tour our New Aseptic Pre-filled Syringe Line

    AMRI Express

    Request a quote for:

  181. Analytical Services
  182. in vitro DMPK Services
  183. Aseptic Fill Finish Services
  184. Antimicrobial discovery testing services
  185. Go to AMRI Express!

    Submit Samples For Analytical Testing

    Learn more about the sample studies we perform and reports we provide.

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    亚博手机客户端|网页版

    News

    John Ratliff Named CEO of AMRI

    2020-02-22

    ALBANY, N.Y.–(BUSINESS WIRE)–AMRI, a leading global pharmaceutical contract research, development and manufacturing organization, today announced that John Ratliff has been...

    News

    AMRI and Metrion Biosciences Collaborate to Offer Ion Channel Drug Discovery Services

    2020-02-22

    ALBANY, N.Y. and CAMBRIDGE, United Kingdom, Sept. 5, 2018 /PRNewswire/ — AMRI, a global contract research, development and manufacturing organization working with the life sciences industry...

    News

    Nemus Bioscience, Inc. Signs Agreement with AMRI to Manufacture Cannabinoid-Based API f...

    2020-02-22

    Long Beach, Calif., Aug. 01, 2020 (GLOBE NEWSWIRE) — Nemus Bioscience, Inc. (OTCQB: NMUS), focused on the development of cannabinoid-based...

    News

    Prakash Pandian Joins AMRI as Chief Information Officer

    2020-02-22

    ALBANY, NY (June 11, 2018) – (PR Newswire) AMRI, a global contract research, development and manufacturing organization working with the...

    Ready to develop a successful partnership?

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  186. Drug Development Solutions
  187. Chemical Process R&D
  188. Continuous Flow Processing
  189. Custom Synthesis
  190. Process Safety Assessment
  191. Scale-up Capabilities
  192. High-Potency APIs (HPAPIs)
  193. Preformulation and Material Science
  194. Physical Characterization
  195. Solid Form Screening and Selection
  196. Enantiomeric Resolution
  197. API Process Integration
  198. Bulk Characterization
  199. Formulation Development
  200. Separations Sciences
  201. Chiral Method Development
  202. Chiral Resolution
  203. Chemical Purification
  204. Impurity Isolation and Identification
  205. Bioanalytical Services
  206. Fine Chemicals
  207. Fine Chemicals Catalog
  208. Vinylphosphonic Acid – VPA
  209. Kilo Lab and Small-Scale Manufacturing
  210. Chemical Development
  211. Technologies and Capabilities
  212. Fermentation, Biocatalysis and Bioprocesses
  213. Organometallic Chemistry
  214. Propanephosphonic Acid Anhydride – T3P®
  215. Vinylphosphonic Acid (VPA)
  216. Analytical Services
  217. Analytical Method Development and Validation
  218. Analytical Testing Services
  219. Sample Submission and Forms
  220. Biopharmaceutical Analysis
  221. Chromatography
  222. Diffraction Studies
  223. Gas Testing
  224. Heavy Metals Testing
  225. Biochemistry Services
  226. Regulatory Aspects of Biological Pharmaceuticals
  227. Biochemical and Biosimilar Characterization
  228. Product-Related Impurity Characterization
  229. Aggregation State Characterization
  230. Structure Elucidation
  231. Protein Formulation Development
  232. Comparability Studies
  233. Protein and Peptide Crystallization
  234. Initial Drug Substance Characterization
  235. Mass Spectrometry
  236. Material Testing
  237. Microbiology
  238. Micromeritics
  239. Microscopy
  240. Personal Care Chemistry
  241. Residual Solvents
  242. Sorption and Desorption
  243. Spectroscopy
  244. Structural Characterization
  245. Thermal Analysis and Calorimetry
  246. Water Analysis
  247. Glass Delamination – USP 1660
  248. Unknown Particulate Identification
  249. Particle Characterization
  250. Batch Release and Stability Lot Testing
  251. Method Development and Validation
  252. Solid-State Chemistry and Particle Engineering
  253. Solid Form Screening and Selection
  254. Crystallization Process Development
  255. Computational Methods
  256. PAT and Pharmaceutical Quality by Design
  257. Drug Product and Delivery
  258. Stability, Solubility, Dissolution
  259. Mapping and Imaging Studies
  260. Formulation Services
  261. In Vitro Bioequivalence Testing
  262. Extractables and Leachables
  263. Chemical Characterization
  264. E&L for Pharma and Biotech
  265. Impurities
  266. Toxicological Risk Assessment (TRA)
  267. Container Closure Integrity
  268. Vacuum Decay Leak Detection
  269. Electrical Conductivity (HVLD)
  270. Helium Leak Detection (HeLD)
  271. Residual Seal Force (RSF)
  272. Mass Flow Leak Detection
  273. Laser-Based Headspace Analysis
  274. Airborne Ultrasound / Seal-Scan
  275. Container Qualification
  276. Pharmaceutical Glass
  277. <USP 661> Plastic Containers
  278. <USP 670> Auxiliary Packaging Components
  279. <USP 671> Container Performance
  280. EP & JP Container Testing
  281. Elastomeric Closures
  282. Biological Reactivity
  283. Container Qualification Full Test List
  284. Packaging and Distribution Testing
  285. ASTM & ISTA Distribution
  286. Environmental Conditioning, Cycling and Simulation Testing
  287. Pharmaceutical Package Testing
  288. Medical Device Packaging Testing
  289. Consumer Product Packaging
  290. Shelf Life and Accelerated Aging Testing
  291. Packaging Materials Testing
  292. Package Labeling
  293. Package Strength
  294. Package Integrity
  295. Retains and Complaint Resolution
  296. Environmental Conditioning
  297. ISTA 6 Amazon Testing
  298. Medical Device Testing
  299. Cleaning Validations
  300. ISO 10993 Biocompatibility
  301. ISO 11607 Medical Device Validation
  302. Mechanical and Functional Device Testing
  303. Leak Detection
  304. Dose Delivery
  305. Syringes
  306. Drug Delivery Device Testing
  307. Functional, Mechanical, & Metrology Testing
  308. Small Bore Connector Testing
  309. Complaint Handling
  310. Microbiological Laboratory
  311. Microbial Limits Testing
  312. Bacterial Endotoxin Testing: USP <85>
  313. Antimicrobial Effectiveness – AET
  314. Microbiological Population Verification
  315. USP <87> Biological Reactivity Tests – In Vitro
  316. Disinfectant Efficacy
  317. Environmental Monitoring
  318. Water Testing
  319. Problem Solving
  320. Patent Prosecution and Litigation Support
  321. Intellectual Property Support
  322. Regulatory Support
  323. Counterfeit Analysis
  324. API Development and Manufacturing Solutions
  325. APIs and Intermediates
  326. Custom Synthesis and Contract Manufacturing
  327. Fine Chemicals
  328. Technologies and Capabilities
  329. Fermentation, Biocatalysis and Bioprocesses
  330. Boronic Acids, Biaryls, Grignards and Organolithiums
  331. Sterile APIs
  332. DEA-Controlled Compounds
  333. High-Potency APIs
  334. Halogenations and Other Hazardous Chemistries
  335. Propanephosphonic Acid Anhydride – T3P®
  336. Regulatory Support and QA
  337. Drug Product Solutions
  338. Drug Product Development Capabilities
  339. Drug Product Manufacturing
  340. Vials
  341. Syringes
  342. Bottles
  343. Lyophilization
  344. Sterile University
  345. Stability and Release Testing
  346. Government Contracting
  347. CAS and other designations
  348. Prime Contracts
  349. Subcontracts
  350. News
  351. Events
  352. AMRI Express
  353. In Vitro DMPK
  354. Antimicrobial Discovery
  355. Let’s Get Started
  356. Link:

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