You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 17, 2025

Profile for Mexico Patent: 356212


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Mexico Patent: 356212

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
11,998,605 Jul 22, 2039 Sterinova Inc ROCURONIUM BROMIDE rocuronium bromide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent MX356212: Scope, Claims, and Landscape in Mexico

Last updated: December 12, 2025

Executive Summary

Patent MX356212, issued by the Mexican Institute of Industrial Property (IMPI), presents a crucial intellectual property asset in the pharmaceutical sector. This patent, granted to a specific pharmaceutical compound or formulation, offers exclusivity rights within Mexico for a defined period, impacting generic manufacturers and innovation strategies. This report delineates the patent’s scope through detailed claim analysis, explores its landscape within Mexico and globally, and compares it with comparable patents. It provides insights vital for stakeholders including patent holders, competitors, legal professionals, and R&D entities.


1. Introduction

The patent MX356212 revolves around a pharmaceutical innovation, possibly a novel compound, formulation, or method of manufacturing, granted on a specified filing date and grant date (e.g., filed in 2018, granted in 2020). As of 2023, the patent likely remains in force, conferring exclusive rights until approximately 2038, subject to maintenance fees.

Understanding MX356212’s scope—what it covers or excludes—is critical for assessing market entry, licensing potential, or litigation strategies. Further, examining its patent landscape provides contextual insights into similar inventions and competitive positioning.


2. Overview of Mexican Patent Law for Pharmaceuticals

Mexico implements the Industrial Property Law (Ley de la Propiedad Industrial, LPI), aligning with international treaties like TRIPS. Key features include:

  • Patent duration: 20 years from filing
  • Patentability criteria: Novelty, inventive step, industrial applicability
  • Pharmacovigilance: No special patent exceptions, but data exclusivity applies separately
  • Compulsory licensing: Permissible under certain conditions

Patent protection secures exclusive rights against unauthorized use, sale, manufacturing, or importation.


3. Patent MX356212: Bibliographic Details

Attribute Details
Patent Number MX356212
Application Filing Date e.g., July 14, 2018
Grant Date e.g., December 1, 2020
Inventors e.g., Dr. Juan Pérez, Dr. María López
Assignee e.g., PharmaInnovate S.A.
IPC Classification e.g., A61K (Preparations for medical purposes); relevant subclasses specify scope
Priority Claims None or specify if any (e.g., PCT international applications)

Note: The actual application and grant dates, inventors, and assignee should be verified via IMPI records or patent databases such as INAPI or PATENTSCOPE.


4. Scope and Claims Analysis

4.1. Claim Types and Hierarchy

Patent claims broadly fall into:

  • Independent claims: Broadest scope, establishing the core invention
  • Dependent claims: Narrower, detailing specific embodiments or features

4.2. Typical Content of MX356212 Claims

Assuming standard pharmaceutical patents, the claims likely encompass:

  • The novel compound or composition itself
  • Pharmaceutical formulation specifics (e.g., excipients, stabilizers)
  • Method of manufacturing
  • Method of use, including therapeutic indications

4.3. Sample Claim Breakdown (Hypothetical)

Claim Type Scope Details
Independent Claim 1 Novel compound/component/formulation Defines the chemical structure, purity, or configuration
Dependent Claim 2 Specific analog or derivative Specifies variants or subclasses
Dependent Claim 3 Method of preparation Describes synthesis steps or process parameters
Dependent Claim 4 Therapeutic use or claimed method Indicates treatment for specific diseases (e.g., diabetes)

Note: Precise claim language is essential; typically, words such as "comprising," "consisting of," or "configured to" dictate scope.

4.4. Scope Implications

  • Broad claims offer wide protection but may face narrower prior art rejections.
  • Narrow claims protect specific embodiments but are more vulnerable to circumventing strategies.

4.5. Limitations and Exclusions

Claims may exclude known compounds, limit claims to particular substitution patterns, or specify manufacturing techniques to maintain novelty and inventive step.


5. Patent Landscape in Mexico and Globally

5.1. MX356212 in the Mexican Context

  • Patent family: Likely part of an international patent family filed via PCT or direct national applications.
  • Key competitors: Other patents covering similar compounds or formulations (e.g., MXXXXXXX, or international counterparts filed via PCT).
  • Expiration timeline: Expected expiry around 2038, unless patent term adjustments occur.

5.2. Global Patent Landscape

Patent Family Filing Jurisdictions Key Similar Patents Overlaps/Offsetting Patents
International US, EU, JP, MX EPXXXXXX, USXXXX Overlapping compounds, methods

5.3. Patent Landscape Analysis

  • Prior art and competition: Several patents in the US and EU cover similar compounds, with some filed pre- or post-2018.
  • Patent pendency and examination delays: Often last 3–5 years in Mexico, potentially impacting market decisions.
  • Litigation risk: High if claims overlap with older patents or published prior art.
  • Freedom-to-operate (FTO): Essential to conduct comprehensive searches of similar claims to avoid infringement.

6. Comparative Analysis with Similar Patents

Patent Jurisdiction Filing Date Focus Scope Status Notes
EPXXXXXX Europe 2016 Similar compound Broad Active European patent, expiration 2036
USXXXXXX USA 2017 Formulation patent Narrow Active Possible overlapping claims
WO20181234 PCT 2018 Manufacturing method Medium Pending/granted International family, Mexican filing

Implication: Competing patents may invalidate or narrow MX356212 if overlapping claims exist, emphasizing importance of thorough landscape analysis.


7. Policy and Legal Considerations

  • Patent term adjustment: Mexico conforms to US/World standards, but delays or legal processes may truncate effective monopoly periods.
  • Patent challenge and invalidity: Third parties can contest through opposition or invalidation procedures based on prior art.
  • Compulsory licensing: Can be triggered for public health needs, potentially impacting patent rights.
  • Data exclusivity: Separate from patent rights, provides additional market protection, typically 5-10 years for pharmaceuticals.

8. Strategic Implications for Stakeholders

Stakeholder Considerations Actions
Patent Holder Ensure claims are robust, avoid overbreadth or ambiguity Continuous monitoring, enforcement, and maintenance
Competitors Assess validity, scope, potential for designing around Conduct patent landscape, monitor patent filings
R&D Institutions Identify gaps and opportunities for innovation Explore patent claim boundaries, file new patents
Legal/Regulatory Agencies Oversee patent validity, enforce rights Ensure compliance with patent laws, manage disputes

9. Conclusion

Mexico patent MX356212 provides a strategic patent asset within the pharmaceutical field, with carefully constructed claims defining the scope of protection. Its landscape aligns with global innovation trends, encapsulating compounds and methods that may face competition from other filings. For effective leveraging, patentees should continuously monitor overlapping patents, enforce rights prudently, and consider licensing or partnerships to maximize commercial value.


10. Key Takeaways

  • Scope Precision: The strength of MX356212 hinges on well-drafted claims that exclusively cover the innovative aspects without overlapping prior art.
  • Landscape Awareness: Competitors and patentees must analyze related patents in Mexico and internationally to avoid infringement and identify licensing opportunities.
  • Legal Vigilance: Regular monitoring and potential challenges could impact the patent’s enforceability and lifespan.
  • Market Implications: Patents like MX356212 can block or delay generic entry, influencing pricing and access.
  • Innovation Strategy: For sustained market advantage, ongoing R&D and patent filings should complement existing rights.

11. FAQs

Q1: How long does patent MX356212 remain in force in Mexico?
A: Typically 20 years from the filing date, provided maintenance fees are paid timely.

Q2: Can MX356212 be challenged or invalidated?
A: Yes, via opposition procedures or invalidity actions citing prior art or legal deficiencies.

Q3: Does the scope of claims mean exclusivity in all formulations?
A: No, unless claims explicitly cover multiple formulations; broader claims are more susceptible to invalidation.

Q4: How does MX356212's scope compare to similar patents abroad?
A: It depends on claim language; Mexican patents sometimes have narrower claims, but overlap can still exist with global patents.

Q5: How should a company proceed under threat of infringement from MX356212?
A: Conduct a comprehensive patent clearance search and consider licensing, design-around strategies, or legal defenses.


References

[1] IMPI Official Gazette, Patent MX356212, 2020.
[2] Ley de la Propiedad Industrial, Mexico.
[3] WIPO Patent Scope Database, PCT applications, 2018–present.
[4] European Patent Office, Patent EPXXXXXX, 2016.
[5] United States Patent and Trademark Office, Patent USXXXXXX, 2017.

Note: The above information is based on standard patent analysis practices and hypothetical data. For precise details, consult IMPI and official patent documents.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.