Complaints Policy
1.1 Policy Statement
At London Health Company (LHC), client feedback is invaluable. We are committed to acknowledging all feedback within 48 hours and resolving complaints as quickly as possible. We take negative feedback and complaints seriously and are dedicated to resolving any service shortcomings to patient’s satisfaction.
1.2 Scope
This policy covers all feedback and complaints regarding LHC's services, received through any channel:
- Verbal: Phone (020 80870017), in-person at branches/testing locations.
- Written: Email (info@lhclab.co.uk and online forms.
- Online Reviews: Trustpilot, Google Reviews, etc.
- Website Contact Forms: LHC websites www.londonhealthcompany.co.uk
This policy operates in conjunction with our Terms and Conditions and Privacy Policy.
- Purpose and Objectives
This policy ensures fair and effective management of client complaints and concerns, driving continuous improvement. It aims to:
- Address complaints promptly and appropriately.
- Learn from each complaint to enhance service quality.
- Inform relevant management of service quality issues.
- Identify areas for staff training and development.
- Document and track all complaints using Matrix Gemini.
- Duties and Responsibilities (Oversight by Quality Manager, with Clinical Lead Exception)
All duties related to complaints handling are overseen and managed by the Quality Manager, except in cases where the complaint concerns the Quality Manager or Lab Manager themselves due to potential bias or subjectivity. In such instances, the complaint will be escalated directly to the Clinical Lead for independent investigation and resolution.
The Quality Manager's responsibilities include:
- Policy Management & Compliance: Developing, implementing, maintaining the complaints policy, and ensuring adherence to relevant regulations.
- Complaints Handling Oversight (Except as Noted Above):
- Overseeing policy implementation, compliance, and effectiveness.
- Investigating and resolving complaints (unless regarding the Quality Manager or Lab Manager).
- Managing policy amendments.
- Ensuring staff training on complaints handling.
- Providing guidance and support to the complaints handling team once applicable.
- Escalating complex or serious complaints (unless regarding the Quality Manager or Lab Manager).
- Monitoring complaint resolution times and adherence to policy timeframes.
- Receiving, logging, and handling initial complaints.
- Promptly acknowledging complaints.
- Gathering information from complainants.
- Attempting first-contact resolution.
- Ensuring immediate notification of formal complaints to the Quality Manager or designated deputy (unless regarding the Quality Manager or Lab Manager).
- Principles of Complaints Handling
LHC adheres to the Parliamentary and Health Service Ombudsman's Six Principles of Good Complaints Handling:
- Getting it Right
- Being Customer-Focused
- Being Open and Accountable
- Acting Fairly and Proportionately
- Putting Things Right
- Seeking Continuous Improvement
- Complaints Procedures
5.1 Definition of a Complaint
A complaint is any expression of dissatisfaction with any aspect of LHC’s services, including:
- Test results/reporting
- Customer service
- Testing processes/procedures
- Communication/information
- Billing/payment
5.2 Timeframes for Response
- Informal Complaints: Resolved quickly, ideally at the first point of contact, aiming for resolution within 48 hours.
- Formal Complaints:
- Acknowledgement: Written acknowledgement within 2 working days.
- Resolution: Aim for resolution within 14 working days. If more time is needed, the complainant will be informed with a revised timeframe.
5.3 Time Limits for Complaints
Complaints should ideally be made within 12 months of the event or becoming aware of the issue. Exceptions may be considered on a case-by-case basis.
5.4 Sources of Complaints
Complaints may be received from:
- Individual clients
- Healthcare professionals (e.g., GPs)
- Organizations (e.g., companies, clinics)
- Members of the public
- LHC staff (via internal channels)
5.5 Receiving Complaints
- Matrix Gemini Logging: All complaints must be logged in MAtrix Gemini.
- Verbal Complaints: If resolved immediately, formal documentation in Matrix Gemini is not required unless requested by the complainant. A brief record of the interaction should be kept.
- Written Complaints: These complaints must be logged into Matrix Gemini logging.
- Online Reviews: Monitor and respond publicly where appropriate, also logging the issue in Matrix Gemini.
5.6 Grading Complaints (Severity Levels)
- Level 1 (Minor): Minor service issues (e.g., minor delays, administrative errors). Handled by the Quality Manager.
- Level 2 (Moderate): More serious service failures (e.g., incorrect results, significant delays). Escalated to the Quality Manager or designated deputy (unless regarding the Quality Manager or Lab Manager).
- Level 3 (Serious): Potentially significant consequences (e.g., serious negligence, confidentiality breaches). Must be dealt with both Quality Manager and lab manager (unless regarding the Quality Manager or Lab Manager).
- Level 4 (Critical): Requiring external reporting (CQC). Managed by the Quality Manager (unless regarding the Quality Manager or Lab Manager) with external reporting as required.
5.7 Complaints Against Senior Management (Including Quality Manager and Lab Manager)
Complaints against senior management, including the Quality Manager and Lab Manager, should be directed to the Clinical Lead.
5.8 Action Plan for Complaints
If a formal complaint cannot be resolved informally, a written action plan will be developed with the complainant, outlining steps and timeframes for resolution (aiming for resolution within 28 days of the plan). This may include a refund or replacement test, where appropriate.
5.9 Investigating and Responding to Complaints
Formal complaints will receive a written response within 28 working days (unless otherwise agreed with the complainant), including:
- Complaint summary
- Investigation description
- Investigation findings
- Actions taken
6. Duty of Candour
For complaints involving notifiable safety incidents, the Duty of Candour procedure will be followed as per the relevant policy.
7.Confidentiality
All complaints will be handled confidentially. Complainants will be informed if access to medical records is required.
8. Unreasonable or Vexatious Complaints
For unreasonable, aggressive, or repeatedly vexatious complainants, the following measures may be applied:
- Single senior contact (typically the Quality Manager or designated deputy, unless the complaint concerns them, in which case it will be the Clinical Lead).
- Restricted communication method (e.g., written only).
- Time limits for contact.
LHC reserves the right to cease responding to resolved or vexatious complaints. This policy ensures fair and thorough complaints handling, reflecting our commitment to continuous service improvement.
Frequently Asked Questions (FAQs)
How is the test performed?
You will receive a complete blood collection kit by post. The kit contains all you need to collect blood from your finger. The components of the kit are:
1. Instruction Sheet: Provides detailed steps on how to collect the blood sample correctly.
2. Box: Contains all the components and is used to hold the tube while collecting blood.
3. Lab Request Form: Needs to be filled out and included with the sample.
4. Labels: For labeling the sample tube.
5. Tube Pouch: A protective pouch for the sample tube.
6. UN3733 Prepaid Mailing Bag: For sending the sample back to the lab.
7. Lancets: Used to prick your finger for blood collection.
8. Wipes: For cleaning your finger before and after collection.
9. Plasters: To cover your finger after blood collection.
10. Blood Collection Tube: for collecting the blood sample.
These components are essential to ensure that the blood sample is collected, stored and sent correctly for accurate testing.
Do I need to set up an account?
No, you don’t need to set up an account, but you do need to activate the sample ID before sending your blood sample to the lab.
Should I fast before collecting my blood sample?
Most of our tests don’t require fasting. However, for accurate results, if you are doing a cholesterol/lipid profile test, fasting is recommended for at least 8 hours, but you can drink water. Non-fasting in this case could lead to triglyceride elevation, especially after a fatty meal as the elevation will be significant.
I couldn’t collect enough blood, what should I do?
If you read the instruction sheet carefully and follow the steps as directed, then you should not have a problem in collecting the right amount of blood. However, if you followed all the steps and couldn’t get enough blood, i.e., to the upper line, please contact us and we will arrange to send you a fresh tube, lancets, wipes and plasters free of charge. Please make sure you keep any unused elements (instruction sheet, box, lab request form, labels, tube pouch, and UN3733 prepaid mailing bag) from the kit as you will need them when you receive the new tube and lancets.
I sent my sample, and the blood wasn’t enough, and I didn’t contact London Health Company. What’s going to happen now?
Don’t send any sample if the blood isn’t enough unless you contactedus and we told you to do so. If you sent the sample and the blood wasn’t enough, the lab will reject your sample and it won’t be processed.
After I closed the yellow tube cap, and inverted it 5-10 times gently, I noticed the waxy substance in the tube didn’t dissolve or move, is this OK?
Yes, this is fine. When inverting the tube, the blood will mix with the waxy substance, but you won’t be able to see any difference. The waxy substance will not move or dissolve.
The yellow-top tube has waxy substance, but the purple top tube looks empty. Is it a faulty tube?
The purple top tube is perfectly fine and should look empty.
Where do I find my sample ID?
Your sample ID is unique and should be on the small lab request slip and is highlighted. Your sample ID should always start with three letters and has no spaces.
What happens if I forgot to activate my sample ID before sending the sample to the lab?
This will cause significant delays in reporting the sample if it arrives at the lab and is not yet activated.
What if I forgot to include the lab request slip/form with my sample?
That shouldn’t be a big problem. You can still receive your report on time, but you need to make sure that the sample ID is activated before the sample arrives at the lab. If the lab request slip/form isn’t included and the sample ID isn’t activated, the lab will discard the sample and no refund will be issued.
I bought my test kit online, does that mean that you have my details, and I don’t need to activate my sample ID?
You still need to activate your sample ID. By activating your sample ID, your blood sample is linked to you. Without activating your sample ID, your blood sample won’t be traced back to you.
Do I need to drop off my blood sample at the post office?
No need to drop it off at the post office; any red letterbox should be fine. Make sure that it’s dropped off before the last collection time; otherwise, it will stay in the letterbox overnight and the lab won’t get it the next day.
Why do I need to avoid posting my blood sample on Friday and weekends?
We aim to receive your blood sample within 24 hours of blood collection. If the sample is posted on a Friday, it means that it will stay in the post for 3 days.
How long does it take for the lab to receive my sample?
Generally, samples arrive within 24 hours of posting to the lab. We use Royal Mail Tracked 24 service, but sometimes, there might be a slight delay in delivery. If the sample’s integrity was compromised by delays, we send a free replacement kit if you have the tracking number to prove the time of posting.
How will I know if my sample was received by the lab?
You will receive an email notification confirming that your sample was checked into the lab.
How will I receive my results?
Once your report is checked and ready, it will be sent to your registered email.
Why have I not received all my results?
This is usually due to one of two reasons:
1. Late or non-activation of the sample ID.
2. Entering the wrong sample ID.
Why does my report say that my sample was rejected by the lab?
Sample rejection mainly occurs due to haemolysis, which is when the red blood cells in the blood collection tube start to break down. This impacts the lab ability to generate results for some tests.
Haemolysis can happen at any stage of the process but most commonly occurs during blood collection. It often results from squeezing your finger instead of massaging the side of your hand. This only happens in a small number of cases, and we will provide a second kit free of charge.
Another reason for sample rejection is when a person has been unable to collect the necessary amount of blood required to perform the testing and sends it to the lab without contacting us beforehand.