SafetyIQ – Global Product Quality Violations and Counterfeit Tracking Software
Services We Offer
SafetyIQ is a platform intended for regulatory affairs, procurement, customs and health authorities for monitoring product quality violations by pharmaceutical, supplements and other life sciences products worldwide. SafetyIQ helps analyse types of product quality violations, product recalls (both voluntary and statutory) to evaluate suitable products and manufacturers for import and procurement purpose.
Regulatory Authorities In Colombia
Assess Global Product Quality Landscape
- Track global alerts related to product quality violations such as packaging issues, labelling issues, contamination, substandard products, quality defects and others
- Assess timelines of alerts globally with markets with high density of violations, source country of imports and type of products
- Analyze global trends related to product quality violations and counterfeit drugs / devices / supplements
Assess Global Manufacturers to Find Suitable Partners and Filter High Risk Suppliers
- SafetyIQ has inbuild risk scoring metric that groups manufacturers, distributors of medicines and other products based on their risk profile
- The risk profile considers type and number of recalls, intentions and several parameters to group the manufacturers and distributors
- A watchlist of manufacturers with potential safety risk
- Compare multiple manufacturers to find suitable candidates for supply
- Review company profile, management members and their associations to evaluate health of the company
How SafetyIQ works?
SafetyIQ is built by Artixio’s inhouse artificial intelligence and machine learning engineers, data scientists. Leveraging leading technologies, Artixio has developed the core logic for evaluating and grouping manufacturers based on their history of violations. They are grouped from no to high-risk categories through risk classification and proprietary risk scoring model. Our engineers have build data pipeline to track and analyse data from authentic health authority websites, new sources and other medicines specific websites. Our AI model has been trained to identify key data points and context to create global database and dashboard powered by backend analytics.
Our Services
Regulatory Affairs
Product Registration
Market Access
IND (Investigational New Drug)
NDA (New Drug Application)
Regulatory Operations
Technical Writing
Regulatory Strategy
Market Access
Why Trust Artixio with Your Regulatory Journey In Colombia?
Local expertise with 15-20 years of experience in successfully registering and maintaining 2000+ licenses
Direct access to in-house INVIMA regulatory liaisons
KPI based, continual process excellence
Successful Approvals and Ongoing Product Lifecycle Maintenance for 200+ products
End-to-end support from concept to commercialization
Our 15-30 years of experience tech-enabled team with a regulatory intelligence-driven solution ensures sustained compliance in Colombia.
Flexible, strategic, timely, and quality submissions.
ISO 9001:2015, Quality Driven Services Platform
Hybrid-Local-Centralized Support across Regulatory functions
FAQs
Who can use SafetyIQ?
Health Authorities and Ministries of Health, Custom Officials regulating medicines, devices products at ports, procurement officers in government, pharmaceutical companies, health networks, NGOs, government bodies, regulatory affairs professionals and others who would like to find suitable manufacturers for pharmaceutical, medical devices, supplements and related products and identify high risk suppliers based on past product quality violations.
How SafetyIQ provides information on product quality violations?
The platform provides dashboards on latest alerts, distribution of alerts in various countries, type of alerts, type of violations, companies watchlist, compare companies, company profiles and other details.
Can I find distributors for my products using SafetyIQ?
Yes, SafetyIQ tracks distributors based on product violation alerts gathered from various sources. QuriousRI also tracks distributors and importers of medicines, supplements and medical devices in global markets based on information available through health authority websites. Using both the tools, manufacturers can search for distributors and evaluate their risk profile for finding suitable partners.
How to use SafetyIQ?
SafetyIQ can help track global counterfeit products identified by manufacturers, health agencies and governments to establish a global watchlist. It can help identify high risk manufacturers with history of supplying poor quality products. Counterfeit and poor-quality medicines result loss of millions of lives worldwide. Concerned officers can use the tool to identify sources of such products to make necessary decisions.
Industries We Serve in the Colombia
Pharmaceuticals
MedTech
Cosmetics
Nutrition
Biologics
Veterinary
Our Global Reach: Serving Life
Sciences Clients Worldwide
India
Singapore
Mexico
Brazil
Vietnam
Malaysia
Argentina
Colombia
Taiwan
China
Europe
Thailand
Indonesia
Philippines
USA
Japan
Qatar
South Korea
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