#labeling compliance

[packagingworldinsights]

Is your organization ready to meet the deadlines for the EU Classification, Labelling, and Packaging (CLP) Regulation updates? If your products fall within the new hazard classifications for chemical.

[thebeautyscientist]

The New EU Allergen List

What’s Changing and Why? Until recently, EU law required cosmetic products to list 24 specific fragrance allergens on their packaging if they were present above very low levels. These rules were designed to help people who are sensitive to certain ingredients avoid products that might cause them problems. However, as our understanding of allergies has improved, it’s become clear that more…

[chemzingraphics]

Printing for pharmaceutical industry

At Chemzin Graphics, we specialize in high-quality, precision-driven printing solutions for the pharmaceutical industry. With a deep understanding of the strict regulatory and branding needs of pharma companies, we deliver printing services that ensure clarity, compliance, and consistency.

From product labels, cartons, leaflets, and blister packaging to customized marketing materials, our advanced printing technology ensures vibrant, durable, and accurate results every time. We prioritize legibility, tamper-evidence, and brand integrity, making us a trusted partner for pharmaceutical manufacturers and PCD franchise companies.

Why Choose Chemzin Graphics?

Expertise in pharma-specific printing standards

GMP & ISO-compliant print processes

Tamper-proof and eco-friendly printing options

Fast turnaround with consistent quality control

Custom design and branding support

Whether you're a small-scale pharma startup or a large-scale exporter, Chemzin Graphics offers reliable, high-quality printing solutions tailored to your pharmaceutical packaging needs.

Chemzin Graphics – Precision Printing for a Safer, Smarter Pharma Industry.

[platinumcrow]

GTM Managed Services for Providers: Why WorkSeer is the Best Trade Compliance Platform for MSPs

In the fast-evolving world of international trade, Managed Service Providers (MSPs) are stepping up to help businesses stay compliant, efficient, and globally connected. But to truly deliver value in today’s complex supply chain environment, MSPs need more than expertise — they need the right tools.

That’s where WorkSeer comes in.

Designed for the modern provider, WorkSeer offers a powerful and customizable GTM Managed Services Platform for Providers — built with white-label capabilities and workflow automation at its core. Whether you're launching new compliance services or scaling existing ones, WorkSeer equips you with everything you need to succeed.

Why GTM Managed Services Are the Future for Providers

With global regulations tightening and trade routes becoming more unpredictable, companies are increasingly turning to MSPs for help with import/export compliance, customs clearance, and global supply chain optimization.

GTM (Global Trade Management) Managed Services allow MSPs to:

Reduce client risk from non-compliance

Improve operational efficiency across borders

Deliver turnkey trade solutions without building infrastructure from scratch

But to deliver these services effectively and profitably, MSPs need a platform that supports automation, branding, integration, and scalability.

WorkSeer: The Best Trade Compliance Platform for MSPs

WorkSeer is not just a GTM tool — it's a complete trade compliance ecosystem, purpose-built for MSPs. Here’s why WorkSeer is the top choice for providers:

 1. White Label Platform

Operate under your own brand with full white-label functionality. From login screens to dashboards, WorkSeer lets you offer a fully customized compliance solution to your clients — as if it were built by your own team.

2. Workflow Automation

WorkSeer automates critical compliance tasks such as:

HS code classification

Denied party screening

Document generation

FTA eligibility and certificate creation

Customs filing support

This reduces manual errors, saves time, and helps MSPs scale operations with fewer resources.

 3. Real-Time Regulatory Compliance

Stay up-to-date with constantly changing global trade regulations. WorkSeer’s compliance engine updates in real-time to reflect changes in tariffs, trade agreements, and customs requirements worldwide.

4. Seamless Client Management

Manage multiple client accounts in one place. The platform supports:

Client-specific workflows

Custom rules and alerts

Secure data segregation

Analytics dashboards for performance tracking

5. Easy Integration

WorkSeer is built API-first, enabling fast integration with ERP systems, logistics platforms, and CRMs — helping MSPs create a connected and seamless service experience for their clients.

Scalable GTM Services Without the Overhead

One of the biggest challenges for MSPs entering the GTM space is the cost and time required to build a secure, scalable system. WorkSeer eliminates that barrier. With low startup costs, fast onboarding, and complete white-label flexibility, providers can go to market in days — not months.

Whether you serve eCommerce clients, freight forwarders, or large enterprises, WorkSeer enables you to deliver high-impact trade compliance services with confidence.

Final Thoughts: The MSP Opportunity Starts with WorkSeer

If you’re an MSP looking to expand your offerings, reduce client risk, and drive new revenue — now is the time to embrace GTM Managed Services for Providers.

With WorkSeer’s white label & workflow automation features, you gain a competitive edge and deliver the kind of compliance-as-a-service solution today’s global businesses demand.

 Want to See WorkSeer in Action?

Get in touch with our team for a personalized demo. 📩 Email: support@workseer.com 🌐 Website: https://www.workseer.com/gtm-managed-services.php

[insightfultake]

Music Labels Strike Back: Influencers Face Heat Over Copyright Violations

India’s influencer boom, long celebrated as a new-age marketing goldmine, is now facing a strong countercurrent from an unlikely quarter—music labels. As digital creators ride the wave of social media clout, their frequent use of copyrighted music in brand-sponsored posts has attracted the ire of the music industry, prompting legal action, content takedowns, and steep fines.

[freyrsolutions]

Ensure legal and safety compliance in the EU for cosmetics; consumer goods. Learn about PIF, CE marking, labeling, RP, & CPNP portal in this step-by-step guide.

[springbordrealestateservices]

🔐 Is your labeling data truly secure? 🔐

In today’s fast-paced, digital world, data security is critical for every business. Whether you're managing compliance data, customer information, or product labeling, a breach could cause major setbacks. But don't worry, Springbord is here to help!

Our secure labeling services ensure your business stays protected from data vulnerabilities. With advanced protocols, employee training, and risk management strategies, we keep your labeling processes safe and compliant. 🚀

Safeguard your data today and ensure your business remains resilient. 🛡️

[bob3160]

FCC’s New ‘Cyber Trust Mark’ - Shining Shield or Shiny Sticker

[freyrnigeria]

Learn about BPOM compliance, cosmetic documentation, import regulations, and product approvals to navigate the Indonesian cosmetic market successfully.

[regulatorysolutionsindia]

A Guide to Legal Metrology Compliance for Medical Devices in India

If you're working with medical devices in India, it's crucial to understand the Legal Metrology Act and its compliance requirements. This guide covers everything from labeling and packaging standards to the necessary regulations for medical device manufacturers, importers, and distributors.

🔑 Key Points:

Overview of the Legal Metrology Act and its impact on medical devices.

Compliance requirements for labeling, packaging, and more.

Tips for navigating common regulatory challenges.

Stay informed and compliant to avoid legal issues and ensure your medical devices meet the required standards. 💼⚖️

[colinwilson11]

Medical Device Labeling: The Important Role Of Medical Device Label In Patient Care

Medical devices sold in the United States must comply with labeling requirements set by the Food and Drug Administration (FDA). All labels must contain specific information about the device such as its intended use, any potential risks or side effects, and instructions for use. Device labels provide critical safety information that helps ensure devices are used properly. The FDA regulates labeling to protect patient health.

Labels Must Clearly Identify The Device

First and foremost, a Medical Device Labeling must clearly identify the specific device. This includes stating the product name and any applicable product codes or reference numbers. Having a clear device name and identification numbers helps providers and facilities properly select, use, and track the intended device. Any trade or brand names must also be included but must not overshadow the core product identity information.

Instructions For Use Must Be Clear And Complete

Detailed instructions for use are extremely important for medical devices to be operated safely and as intended. Labels must provide step-by-step directions on how the device is to be used, prepared, fitted, applied, implanted, or operated. Pictures, diagrams or other illustrative guides can help visualize proper technique when words alone may not fully explain the process. Instructions must account for all reasonably foreseeable uses. Omitting any necessary steps could result in misuse leading to patient harm.

Packaging Labels Provide Sterility And Shelf Life Assurances

For devices distributed in single-use sterile packaging, labels must affirm the method used to sterilize the contents as well as the expiration date or shelf life. This information guarantees the continued sterility and integrity of the device up until the noted expiration date. Devices like surgical tools and implants must remain free of contaminants when used. Packaging labels demonstrate the steps taken to achieve and maintain sterile conditions.

Potential Adverse Reactions And Hazards Must Be Disclosed

Device labels must include a complete list of known or reasonably foreseeable adverse health effects or hazards from use. This involves describing any potential allergic reactions, biological risks, toxicology concerns and interactions with other devices, drugs or substances. Precautions, contraindications and any use limitations due to patient risks or conditions should also be detailed. Making providers aware of safety issues enables them to properly assess risks and benefits for individual patients.

Symbols Standardize Hazard And Safety Communications

Pictograms and symbols play an important role in medical device labeling by allowing concepts to be recognized universally without language barriers. Common symbols indicate requirements such as “Do Not Reuse”, “Sterilized Using Irradiation”, “Keep Away From Heat or Flames”, and many others defined by International Standards Organization (ISO) regulations. Having standardized symbols helps labeling information be consistently interpreted.

Product Labels Remain With The Device

Device manufacturers must ensure all labeling remains affixed or adjacent to the medical device itself throughout distribution and use. Shipping labels serve to identify devices during transportation but do not replace the requirement for complete labeling on the finished able product. Device labels need to be available anytime and anywhere the device is utilized to provide critical use and safety guidance to providers.

As described, medical device labelingserves the fundamental purpose of guiding appropriate and safe use while communicating potential risks. Complying with comprehensive FDA labeling policies supports quality patient care.

Get more insights on this topic:   https://www.pressreleasebulletin.com/medical-device-labeling-device-labeling-regulations-ensuring-patient-safety-and-compliance/

About Author:

Ravina Pandya, Content Writer, has a strong foothold in the market research industry. She specializes in writing well-researched articles from different industries, including food and beverages, information and technology, healthcare, chemical and materials, etc. (https://www.linkedin.com/in/ravina-pandya-1a3984191)

*Note: 1. Source: Coherent Market Insights, Public sources, Desk research 2. We have leveraged AI tools to mine information and compile it

[seemabhatnagar]

"UP High Court Upholds Food Safety Standards: Sugandhit Supari Classified as Food Product Under FSSA, 2006"

The court held that "sugandhit supari" is classified as a food item under the Food Safety Standards Act, 2006, and not merely a tobacco product under the Cigarettes and Other Tobacco Products Act, 2003. The summoning order passed by Additional Session Judge Jhasi and the non-bailable warrant issued by Additional District Judge Jhasi were upheld. The application under Section 482 Cr.P.C. for quashing these orders was dismissed.

Jagdish Prasad & Another v. State of UP & Another

Crl. Misc. Case No.11772/2024

Before the High Court of Allahabad

Heard by Hon’ble Mr. Justice Arun Kumar Singh Deshwal J

Fact:

The applicants firm M/s Balaji Traders Orai was involved in the manufacturing and sale of a product named "sugandhit supari".

An inspection was conducted by the Food Security Officer on 20.02.2020 at the manufacturing unit of the firm.

During the inspection, 370 packets of "sugandhit supari" were found, four of which were purchased and sent for analysis.

The food analyst's report indicated that the product contained tobacco, was of substandard quality, and did not meet labeling requirements.

A complaint was filed, leading to the summoning of the applicants and the issuance of a non-bailable warrant.

Legal Issue

Whether "sugandhit supari" is classified as a tobacco product or a food item under the relevant laws.

Whether the proceedings under the Food Safety and Standards Act, 2006 (FSSA, 2006) are valid if "sugandhit supari" is a tobacco product.

Point of arguments

Applicant's argument

"Sugandhit supari" is a tobacco product, and thus proceedings under the FSSA, 2006 are erroneous.

The product should be regulated under the Cigarettes and Other Tobacco Products Act, 2003 (COTPA, 2003).

Even if considered a food item, the applicants hold a valid license, making the invocation of the FSSA, 2006 incorrect.

Opposite Party's Argument

"Sugandhit supari" is a food item and thus falls under the purview of the FSSA, 2006.The applicants failed to present a valid license at the time of inspection.

Court's Observation

The FSSA, 2006 regulates food items to ensure safety for human consumption, while the COTPA, 2003 focuses on regulating and controlling tobacco product.

It considered the inclusion of betel nut (supari) under the definition of food and primary food in the FSSA, 2006 and its standards under the Food Safety and Standards (Food Products Standards and Food Additives) Regulations, 2011.

Food Safety and Standards Act, 2006: Defines "food" as any substance intended for human consumption and includes primary food (Section 3(1)(j)). Betel nut falls under this category as it is a primary food product derived from agriculture.

COTPA, 2003: Regulates tobacco products listed in its schedule. Betel nut (supari) is not listed as a tobacco product under COTPA, 2003 unless it contains tobacco as an ingredient.

[freyrsolutions]

Ensure legal and safety compliance in the EU for cosmetics; consumer goods. Learn about PIF, CE marking, labeling, RP, & CPNP portal in this step-by-step guide.